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dbVar

Database of genomic structural variation

nsv4411090

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:131,084

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 54 studies. See in: genome view

Remapped(Score: Perfect):95,626,108-95,757,191

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
nsv4411090	Remapped	Perfect	GRCh38.p12	Primary Assembly	First Pass	NC_000002.12	Chr2	95,626,108	95,628,495	95,741,512	95,757,191
nsv4411090	Submitted genomic		GRCh37 (hg19)	Primary Assembly		NC_000002.11	Chr2	96,291,856	96,294,243	96,407,260	96,422,939

Variant Call Information

Variant Call ID	Type	Method	Analysis
nssv15710559	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
nssv15710559	Remapped	Perfect	NC_000002.12:g.(95 626108_95628495)_( 95741512_95757191) dup	GRCh38.p12	First Pass	NC_000002.12	Chr2	95,626,108	95,628,495	95,741,512	95,757,191
nssv15710559	Submitted genomic		NC_000002.11:g.(96 291856_96294243)_( 96407260_96422939) dup	GRCh37 (hg19)		NC_000002.11	Chr2	96,291,856	96,294,243	96,407,260	96,422,939

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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