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dbVar

Database of genomic structural variation

nsv5983725

Organism: Homo sapiens

Study:nstd212 (Wu et al. 2021)
Variant Type:copy number variation
Method Type:Sequencing
Submitted on:GRCh38

Variant Calls:1
Validation:Not tested
Clinical Assertions: No
Region Size:73

Publication(s):Wu et al. 2021

Links to Other Resources

Overlapping Genes

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: 127 SVs from 34 studies. See in: genome view

Submitted genomic27,373,612-27,373,684

Variant Region Placement Information

Variant Region ID	Placement Type	Score	Assembly	Assembly Unit	Reciprocity	Sequence ID	Chr	Start	Stop
nsv5983725	Submitted genomic		GRCh38 (hg38)	Primary Assembly		NC_000001.11	Chr1	27,373,612	27,373,684
nsv5983725	Remapped	Perfect	GRCh37.p13	Primary Assembly	First Pass	NC_000001.10	Chr1	27,700,103	27,700,175

Variant Call Information

Variant Call ID	Type	Method	Analysis
nssv17530585	deletion	Sequencing	Sequence alignment

Variant Call Placement Information

Variant Call ID	Placement Type	Score	HGVS	Assembly	Reciprocity	Sequence ID	Chr	Start	Stop
nssv17530585	Submitted genomic		NC_000001.11:g.273 73612_27373684del	GRCh38 (hg38)		NC_000001.11	Chr1	27,373,612	27,373,684
nssv17530585	Remapped	Perfect	NC_000001.10:g.277 00103_27700175del	GRCh37.p13	First Pass	NC_000001.10	Chr1	27,700,103	27,700,175

No validation data were submitted for this variant

No clinical assertion data were submitted for this variant

Genotype and/or allele frequency data can be found on dbVar's FTP site.

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