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dbVar

Database of genomic structural variation

nsv4395632

Organism: Homo sapiens

Study:nstd174 (DGV Gold Standard)
Variant Type:copy number variation
Method Type:Multiple
Submitted on:GRCh37 (hg19)

Variant Calls:1
Validation:Not tested
Clinical Assertions: No
Region Size:1,844

Links to Other Resources

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: 135 SVs from 25 studies. See in: genome view

Remapped(Score: Perfect):63,784,948-63,786,791

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
nsv4395632	Remapped	Perfect	GRCh38.p12	Primary Assembly	First Pass	NC_000008.11	Chr8	63,784,948	63,784,950	63,786,756	63,786,791
nsv4395632	Submitted genomic		GRCh37 (hg19)	Primary Assembly		NC_000008.10	Chr8	64,697,505	64,697,507	64,699,313	64,699,348

Variant Call Information

Variant Call ID	Type	Method	Analysis
nssv15742748	copy number loss	Multiple	Multiple

Variant Call Placement Information

Variant Call ID	Placement Type	Score	HGVS	Assembly	Reciprocity	Sequence ID	Chr	Outer Start	Inner Start	Inner Stop	Outer Stop
nssv15742748	Remapped	Perfect	NC_000008.11:g.(63 784948_63784950)_( 63786756_63786791) del	GRCh38.p12	First Pass	NC_000008.11	Chr8	63,784,948	63,784,950	63,786,756	63,786,791
nssv15742748	Submitted genomic		NC_000008.10:g.(64 697505_64697507)_( 64699313_64699348) del	GRCh37 (hg19)		NC_000008.10	Chr8	64,697,505	64,697,507	64,699,313	64,699,348

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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