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dbVar

Database of genomic structural variation

nsv6135696

Organism: Homo sapiens

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

Variant Calls:1
Validation:Not tested
Clinical Assertions: No
Region Size:56,790

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: 3100 SVs from 94 studies. See in: genome view

Remapped(Score: Perfect):32,472,601-32,529,390

Variant Region Placement Information

Variant Region ID	Placement Type	Score	Assembly	Assembly Unit	Reciprocity	Sequence ID	Chr	Outer Start	Inner Start	Inner Stop	Outer Stop
nsv6135696	Remapped	Perfect	GRCh38.p12	Primary Assembly	First Pass	NC_000006.12	Chr6	32,472,601	32,472,612	32,529,389	32,529,390
nsv6135696	Submitted genomic		GRCh37 (hg19)	Primary Assembly		NC_000006.11	Chr6	32,440,378	32,440,389	32,497,166	32,497,167

Variant Call Information

Variant Call ID	Type	Sample ID	Method	Analysis	Other Calls in this Sample and Study
nssv17683404	duplication	SAMN20524661	Sequencing	Paired-end mapping	62

Variant Call Placement Information

Variant Call ID	Placement Type	Score	HGVS	Assembly	Reciprocity	Sequence ID	Chr	Outer Start	Inner Start	Inner Stop	Outer Stop
nssv17683404	Remapped	Perfect	NC_000006.12:g.(32 472601_32472612)_( 32529389_32529390) dup	GRCh38.p12	First Pass	NC_000006.12	Chr6	32,472,601	32,472,612	32,529,389	32,529,390
nssv17683404	Submitted genomic		NC_000006.11:g.(32 440378_32440389)_( 32497166_32497167) dup	GRCh37 (hg19)		NC_000006.11	Chr6	32,440,378	32,440,389	32,497,166	32,497,167

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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