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dbVar

Database of genomic structural variation

nsv4425434

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:43,190

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: 262 SVs from 55 studies. See in: genome view

Remapped(Score: Good):72,136,751-72,179,940

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
nsv4425434	Remapped	Good	GRCh38.p12	Primary Assembly	First Pass	NC_000011.10	Chr11	72,136,751	72,136,751	72,179,940	72,179,940
nsv4425434	Submitted genomic		GRCh37 (hg19)	Primary Assembly		NC_000011.9	Chr11	71,847,797	71,853,982	71,890,685	71,890,984

Variant Call Information

Variant Call ID	Type	Method	Analysis
nssv15708768	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
nssv15708768	Remapped	Good	NC_000011.10:g.(72 136751_72136751)_( 72179940_72179940) dup	GRCh38.p12	First Pass	NC_000011.10	Chr11	72,136,751	72,136,751	72,179,940	72,179,940
nssv15708768	Submitted genomic		NC_000011.9:g.(718 47797_71853982)_(7 1890685_71890984)d up	GRCh37 (hg19)		NC_000011.9	Chr11	71,847,797	71,853,982	71,890,685	71,890,984

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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