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dbVar

Database of genomic structural variation

nsv5987079

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:524,968

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: 1887 SVs from 95 studies. See in: genome view

Submitted genomic194,771,094-195,296,061

Variant Region Placement Information

Variant Region ID	Placement Type	Score	Assembly	Assembly Unit	Reciprocity	Sequence ID	Chr	Start	Stop
nsv5987079	Submitted genomic		GRCh38 (hg38)	Primary Assembly		NC_000002.12	Chr2	194,771,094	195,296,061
nsv5987079	Remapped	Perfect	GRCh37.p13	Primary Assembly	First Pass	NC_000002.11	Chr2	195,635,818	196,160,785

Variant Call Information

Variant Call ID	Type	Method	Analysis
nssv17524131	duplication	Sequencing	Sequence alignment

Variant Call Placement Information

Variant Call ID	Placement Type	Score	HGVS	Assembly	Reciprocity	Sequence ID	Chr	Start	Stop
nssv17524131	Submitted genomic		NC_000002.12:g.194 771094_195296061du p	GRCh38 (hg38)		NC_000002.12	Chr2	194,771,094	195,296,061
nssv17524131	Remapped	Perfect	NC_000002.11:g.195 635818_196160785du p	GRCh37.p13	First Pass	NC_000002.11	Chr2	195,635,818	196,160,785

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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