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dbVar

Database of genomic structural variation

nsv4406025

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:583,986

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: 2417 SVs from 103 studies. See in: genome view

Remapped(Score: Perfect):62,705,123-63,289,108

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
nsv4406025	Remapped	Perfect	GRCh38.p12	Primary Assembly	First Pass	NC_000004.12	Chr4	62,705,123	62,716,405	63,272,594	63,289,108
nsv4406025	Submitted genomic		GRCh37 (hg19)	Primary Assembly		NC_000004.11	Chr4	63,570,841	63,582,123	64,138,312	64,154,826

Variant Call Information

Variant Call ID	Type	Method	Analysis
nssv15711512	copy number gain	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
nssv15711512	Remapped	Perfect	NC_000004.12:g.(62 705123_62716405)_( 63272594_63289108) dup	GRCh38.p12	First Pass	NC_000004.12	Chr4	62,705,123	62,716,405	63,272,594	63,289,108
nssv15711512	Submitted genomic		NC_000004.11:g.(63 570841_63582123)_( 64138312_64154826) dup	GRCh37 (hg19)		NC_000004.11	Chr4	63,570,841	63,582,123	64,138,312	64,154,826

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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