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dbVar

Database of genomic structural variation

nsv4421449

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:943

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: 84 SVs from 29 studies. See in: genome view

Remapped(Score: Perfect):73,203,051-73,203,993

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
nsv4421449	Remapped	Perfect	GRCh38.p12	Primary Assembly	First Pass	NC_000011.10	Chr11	73,203,051	73,203,051	73,203,992	73,203,993
nsv4421449	Submitted genomic		GRCh37 (hg19)	Primary Assembly		NC_000011.9	Chr11	72,914,096	72,914,096	72,915,037	72,915,038

Variant Call Information

Variant Call ID	Type	Method	Analysis
nssv15718202	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
nssv15718202	Remapped	Perfect	NC_000011.10:g.(73 203051_73203051)_( 73203992_73203993) del	GRCh38.p12	First Pass	NC_000011.10	Chr11	73,203,051	73,203,051	73,203,992	73,203,993
nssv15718202	Submitted genomic		NC_000011.9:g.(729 14096_72914096)_(7 2915037_72915038)d el	GRCh37 (hg19)		NC_000011.9	Chr11	72,914,096	72,914,096	72,915,037	72,915,038

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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