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dbVar

Database of genomic structural variation

nsv4430058

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:153,788

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: 990 SVs from 76 studies. See in: genome view

Remapped(Score: Perfect):82,267,669-82,421,456

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
nsv4430058	Remapped	Perfect	GRCh38.p12	Primary Assembly	First Pass	NC_000017.11	Chr17	82,267,669	82,275,977	82,415,061	82,421,456
nsv4430058	Submitted genomic		GRCh37 (hg19)	Primary Assembly		NC_000017.10	Chr17	80,225,545	80,233,853	80,372,937	80,379,332

Variant Call Information

Variant Call ID	Type	Method	Analysis
nssv15710000	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
nssv15710000	Remapped	Perfect	NC_000017.11:g.(82 267669_82275977)_( 82415061_82421456) dup	GRCh38.p12	First Pass	NC_000017.11	Chr17	82,267,669	82,275,977	82,415,061	82,421,456
nssv15710000	Submitted genomic		NC_000017.10:g.(80 225545_80233853)_( 80372937_80379332) dup	GRCh37 (hg19)		NC_000017.10	Chr17	80,225,545	80,233,853	80,372,937	80,379,332

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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