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dbVar

Database of genomic structural variation

esv1667826

Organism: Homo sapiens

Study:estd22 (Levy et al. 2007)
Variant Type:inversion
Method Type:Sequencing
Submitted on:NCBI36 (hg18)

Variant Calls:1
Validation:Not tested
Clinical Assertions: No
Region Size:1,675

Publication(s):Levy et al. 2007

Links to Other Resources

Overlapping Genes

Source: NCBI

Genome View
Variant Region Details and Evidence
Validation Information
Clinical Assertions
Genotype Information

Genome View

Select assembly:

Overlapping variant regions from other studies: 133 SVs from 39 studies. See in: genome view

Remapped(Score: Perfect):106,721,331-106,723,005

Variant Region Placement Information

Variant Region ID	Placement Type	Score	Assembly	Assembly Unit	Reciprocity	Sequence ID	Chr	Start	Stop
esv1667826	Remapped	Perfect	GRCh38.p12	Primary Assembly	First Pass	NC_000006.12	Chr6	106,721,331	106,723,005
esv1667826	Remapped	Perfect	GRCh37.p13	Primary Assembly	Second Pass	NC_000006.11	Chr6	107,169,206	107,170,880
esv1667826	Remapped	Perfect	GRCh37.p13	PATCHES	First Pass	NW_004504300.1	Chr6\|NW_00 4504300.1	25,954	27,628
esv1667826	Submitted genomic		NCBI36 (hg18)	Primary Assembly		NC_000006.10	Chr6	107,275,899	107,277,573

Variant Call Information

Variant Call ID	Type	Sample ID	Method	Analysis	Other Calls in this Sample and Study
essv4361689	inversion	HuRef	Sequencing	Sequence alignment	780,358

Variant Call Placement Information

Variant Call ID	Placement Type	Score	HGVS	Assembly	Reciprocity	Sequence ID	Chr	Start	Stop
essv4361689	Remapped	Perfect	NC_000006.12:g.106 721331_106723005in v	GRCh38.p12	First Pass	NC_000006.12	Chr6	106,721,331	106,723,005
essv4361689	Remapped	Perfect	NW_004504300.1:g.2 5954_27628inv	GRCh37.p13	First Pass	NW_004504300.1	Chr6\|NW_00 4504300.1	25,954	27,628
essv4361689	Remapped	Perfect	NC_000006.11:g.107 169206_107170880in v	GRCh37.p13	Second Pass	NC_000006.11	Chr6	107,169,206	107,170,880
essv4361689	Submitted genomic		NC_000006.10:g.107 275899_107277573in v	NCBI36 (hg18)		NC_000006.10	Chr6	107,275,899	107,277,573

No validation data were submitted for this variant

No clinical assertion data were submitted for this variant

No genotype data were submitted for this variant

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