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dbVar

Database of genomic structural variation

nsv499794

Organism: Homo sapiens

Study:nstd47 (Kidd et al. 2010b)
Variant Type:inversion
Method Type:Sequencing
Submitted on:NCBI36 (hg18)

Variant Calls:1
Validation:Not tested
Clinical Assertions: No
Region Size:54,826

Publication(s):Kidd et al. 2010

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: 323 SVs from 30 studies. See in: genome view

Remapped(Score: Perfect):21,010,649-21,065,474

Variant Region Placement Information

Variant Region ID	Placement Type	Score	Assembly	Assembly Unit	Reciprocity	Sequence ID	Chr	Start	Stop
nsv499794	Remapped	Perfect	GRCh38.p12	Primary Assembly	First Pass	NC_000024.10	ChrY	21,010,649	21,065,474
nsv499794	Remapped	Perfect	GRCh37.p13	Primary Assembly	First Pass	NC_000024.9	ChrY	23,172,535	23,227,360
nsv499794	Submitted genomic		NCBI36 (hg18)	Primary Assembly		NC_000024.8	ChrY	21,581,923	21,636,748

Variant Call Information

Variant Call ID	Type	Method	Analysis
nssv585599	inversion	Sequencing	Sequence alignment

Variant Call Placement Information

Variant Call ID	Placement Type	Score	HGVS	Assembly	Reciprocity	Sequence ID	Chr	Start	Stop
nssv585599	Remapped	Perfect	NC_000024.10:g.210 10649_21065474inv	GRCh38.p12	First Pass	NC_000024.10	ChrY	21,010,649	21,065,474
nssv585599	Remapped	Perfect	NC_000024.9:g.2317 2535_23227360inv	GRCh37.p13	First Pass	NC_000024.9	ChrY	23,172,535	23,227,360
nssv585599	Submitted genomic		NC_000024.8:g.2158 1923_21636748inv	NCBI36 (hg18)		NC_000024.8	ChrY	21,581,923	21,636,748

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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