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dbVar

Database of genomic structural variation

nsv4420802

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:365,166

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: 1500 SVs from 87 studies. See in: genome view

Remapped(Score: Perfect):7,091,816-7,456,981

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
nsv4420802	Remapped	Perfect	GRCh38.p12	Primary Assembly	First Pass	NC_000017.11	Chr17	7,091,816	7,119,404	7,374,368	7,456,981
nsv4420802	Submitted genomic		GRCh37 (hg19)	Primary Assembly		NC_000017.10	Chr17	6,995,135	7,022,723	7,277,687	7,360,300

Variant Call Information

Variant Call ID	Type	Method	Analysis
nssv15724636	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
nssv15724636	Remapped	Perfect	NC_000017.11:g.(70 91816_7119404)_(73 74368_7456981)del	GRCh38.p12	First Pass	NC_000017.11	Chr17	7,091,816	7,119,404	7,374,368	7,456,981
nssv15724636	Submitted genomic		NC_000017.10:g.(69 95135_7022723)_(72 77687_7360300)del	GRCh37 (hg19)		NC_000017.10	Chr17	6,995,135	7,022,723	7,277,687	7,360,300

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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