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dbVar

Database of genomic structural variation

nsv1151457

Organism: Homo sapiens

Study:nstd107 (John et al. 2014)
Variant Type:translocation
Method Type:Sequencing
Submitted on:GRCh37 (hg19)

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

Publication(s):John et al. 2014

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: 174 SVs from 29 studies. See in: genome view

Remapped(Score: Perfect):79,507,633-79,507,633

Variant Region Placement Information

Variant Region ID	Placement Type	Score	Assembly	Assembly Unit	Reciprocity	Sequence ID	Chr	Start	Stop	strand
nsv1151457	Remapped	Perfect	GRCh38.p12	Primary Assembly	First Pass	NC_000013.11	Chr13	79,507,633	79,507,633	-
nsv1151457	Remapped	Perfect	GRCh38.p12	Primary Assembly	First Pass	NC_000014.9	Chr14	58,577,665	58,577,665	+
nsv1151457	Submitted genomic		GRCh37 (hg19)	Primary Assembly		NC_000013.10	Chr13	80,081,768	80,081,768	-
nsv1151457	Submitted genomic		GRCh37 (hg19)	Primary Assembly		NC_000014.8	Chr14	59,044,383	59,044,383	+

Variant Call Information

Variant Call ID	Type	Sample ID	Method	Analysis	Other Calls in this Sample and Study
nssv4004024	interchromosomal translocation	KWB1	Sequencing	Read depth and paired-end mapping	8,440

Variant Call Placement Information

Variant Call ID	Placement Type	Score	Assembly	Reciprocity	Sequence ID	Chr	Start	Stop	strand
nssv4004024	Remapped	Perfect	GRCh38.p12	First Pass	NC_000013.11	Chr13	79,507,633	79,507,633	-
nssv4004024	Remapped	Perfect	GRCh38.p12	First Pass	NC_000014.9	Chr14	58,577,665	58,577,665	+
nssv4004024	Submitted genomic		GRCh37 (hg19)		NC_000013.10	Chr13	80,081,768	80,081,768	-
nssv4004024	Submitted genomic		GRCh37 (hg19)		NC_000014.8	Chr14	59,044,383	59,044,383	+

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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