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dbVar

Database of genomic structural variation

nsv4403897

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:20,481

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: 279 SVs from 66 studies. See in: genome view

Remapped(Score: Perfect):155,760,377-155,780,857

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
nsv4403897	Remapped	Perfect	GRCh38.p12	Primary Assembly	First Pass	NC_000003.12	Chr3	155,760,377	155,760,377	155,780,857	155,780,857
nsv4403897	Submitted genomic		GRCh37 (hg19)	Primary Assembly		NC_000003.11	Chr3	155,478,166	155,478,166	155,498,646	155,498,646

Variant Call Information

Variant Call ID	Type	Method	Analysis
nssv15733094	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
nssv15733094	Remapped	Perfect	NC_000003.12:g.(15 5760377_155760377) _(155780857_155780 857)del	GRCh38.p12	First Pass	NC_000003.12	Chr3	155,760,377	155,760,377	155,780,857	155,780,857
nssv15733094	Submitted genomic		NC_000003.11:g.(15 5478166_155478166) _(155498646_155498 646)del	GRCh37 (hg19)		NC_000003.11	Chr3	155,478,166	155,478,166	155,498,646	155,498,646

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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