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dbVar

Database of genomic structural variation

nsv6137537

Organism: Homo sapiens

Study:nstd213 (Pham et al. 2021)
Variant Type:translocation
Method Type:Sequencing
Submitted on:GRCh37

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

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: 169 SVs from 19 studies. See in: genome view

Remapped(Score: Perfect):77,707,868-77,707,868

Variant Region Placement Information

Variant Region ID	Placement Type	Score	Assembly	Assembly Unit	Reciprocity	Sequence ID	Chr	Start	Stop	strand
nsv6137537	Remapped	Perfect	GRCh38.p12	Primary Assembly	First Pass	NC_000013.11	Chr13	77,707,868	77,707,868	-
nsv6137537	Remapped	Perfect	GRCh38.p12	Primary Assembly	First Pass	NC_000013.11	Chr13	86,038,657	86,038,657	-
nsv6137537	Submitted genomic		GRCh37 (hg19)	Primary Assembly		NC_000013.10	Chr13	78,282,003	78,282,003	-
nsv6137537	Submitted genomic		GRCh37 (hg19)	Primary Assembly		NC_000013.10	Chr13	86,612,792	86,612,792	-

Variant Call Information

Variant Call ID	Type	Sample ID	Method	Analysis	Other Calls in this Sample and Study
nssv17679195	intrachromosomal translocation	SAMN20524665	Sequencing	Paired-end mapping	405

Variant Call Placement Information

Variant Call ID	Placement Type	Score	Assembly	Reciprocity	Sequence ID	Chr	Start	Stop	strand
nssv17679195	Remapped	Perfect	GRCh38.p12	First Pass	NC_000013.11	Chr13	77,707,868	77,707,868	-
nssv17679195	Remapped	Perfect	GRCh38.p12	First Pass	NC_000013.11	Chr13	86,038,657	86,038,657	-
nssv17679195	Submitted genomic		GRCh37 (hg19)		NC_000013.10	Chr13	78,282,003	78,282,003	-
nssv17679195	Submitted genomic		GRCh37 (hg19)		NC_000013.10	Chr13	86,612,792	86,612,792	-

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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