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dbVar

Database of genomic structural variation

nsv4400178

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:389,794

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: 1964 SVs from 92 studies. See in: genome view

Remapped(Score: Perfect):189,255,731-189,645,524

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
nsv4400178	Remapped	Perfect	GRCh38.p12	Primary Assembly	First Pass	NC_000001.11	Chr1	189,255,731	189,255,731	189,645,524	189,645,524
nsv4400178	Submitted genomic		GRCh37 (hg19)	Primary Assembly		NC_000001.10	Chr1	189,224,862	189,321,512	189,545,020	189,614,654

Variant Call Information

Variant Call ID	Type	Method	Analysis
nssv15715438	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
nssv15715438	Remapped	Perfect	NC_000001.11:g.(18 9255731_189255731) _(189645524_189645 524)del	GRCh38.p12	First Pass	NC_000001.11	Chr1	189,255,731	189,255,731	189,645,524	189,645,524
nssv15715438	Submitted genomic		NC_000001.10:g.(18 9224862_189321512) _(189545020_189614 654)del	GRCh37 (hg19)		NC_000001.10	Chr1	189,224,862	189,321,512	189,545,020	189,614,654

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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