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dbVar

Database of genomic structural variation

nsv4427813

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:86

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: 130 SVs from 33 studies. See in: genome view

Remapped(Score: Perfect):23,624,850-23,624,935

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
nsv4427813	Remapped	Perfect	GRCh38.p12	Primary Assembly	First Pass	NC_000020.11	Chr20	23,624,850	23,624,855	23,624,929	23,624,935
nsv4427813	Submitted genomic		GRCh37 (hg19)	Primary Assembly		NC_000020.10	Chr20	23,605,487	23,605,492	23,605,566	23,605,572

Variant Call Information

Variant Call ID	Type	Method	Analysis
nssv15730149	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
nssv15730149	Remapped	Perfect	NC_000020.11:g.(23 624850_23624855)_( 23624929_23624935) del	GRCh38.p12	First Pass	NC_000020.11	Chr20	23,624,850	23,624,855	23,624,929	23,624,935
nssv15730149	Submitted genomic		NC_000020.10:g.(23 605487_23605492)_( 23605566_23605572) del	GRCh37 (hg19)		NC_000020.10	Chr20	23,605,487	23,605,492	23,605,566	23,605,572

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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