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dbVar

Database of genomic structural variation

nsv6001494

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:159,304

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: 616 SVs from 67 studies. See in: genome view

Submitted genomic55,687,159-55,846,462

Variant Region Placement Information

Variant Region ID	Placement Type	Score	Assembly	Assembly Unit	Reciprocity	Sequence ID	Chr	Start	Stop
nsv6001494	Submitted genomic		GRCh38 (hg38)	Primary Assembly		NC_000010.11	Chr10	55,687,159	55,846,462
nsv6001494	Remapped	Perfect	GRCh37.p13	Primary Assembly	First Pass	NC_000010.10	Chr10	57,446,919	57,606,222

Variant Call Information

Variant Call ID	Type	Method	Analysis
nssv17581200	deletion	Sequencing	Sequence alignment

Variant Call Placement Information

Variant Call ID	Placement Type	Score	HGVS	Assembly	Reciprocity	Sequence ID	Chr	Start	Stop
nssv17581200	Submitted genomic		NC_000010.11:g.556 87159_55846462del	GRCh38 (hg38)		NC_000010.11	Chr10	55,687,159	55,846,462
nssv17581200	Remapped	Perfect	NC_000010.10:g.574 46919_57606222del	GRCh37.p13	First Pass	NC_000010.10	Chr10	57,446,919	57,606,222

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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