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dbVar

Database of genomic structural variation

nsv4413158

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:60,316

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: 490 SVs from 60 studies. See in: genome view

Remapped(Score: Perfect):141,142-201,457

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
nsv4413158	Remapped	Perfect	GRCh38.p12	Primary Assembly	First Pass	NC_000020.11	Chr20	141,142	149,678	201,449	201,457
nsv4413158	Submitted genomic		GRCh37 (hg19)	Primary Assembly		NC_000020.10	Chr20	121,783	130,319	182,090	182,098

Variant Call Information

Variant Call ID	Type	Method	Analysis
nssv15729882	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
nssv15729882	Remapped	Perfect	NC_000020.11:g.(14 1142_149678)_(2014 49_201457)del	GRCh38.p12	First Pass	NC_000020.11	Chr20	141,142	149,678	201,449	201,457
nssv15729882	Submitted genomic		NC_000020.10:g.(12 1783_130319)_(1820 90_182098)del	GRCh37 (hg19)		NC_000020.10	Chr20	121,783	130,319	182,090	182,098

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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