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dbVar

Database of genomic structural variation

nsv6032957

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:161

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: 118 SVs from 37 studies. See in: genome view

Submitted genomic46,386,979-46,387,139

Variant Region Placement Information

Variant Region ID	Placement Type	Score	Assembly	Assembly Unit	Reciprocity	Sequence ID	Chr	Start	Stop
nsv6032957	Submitted genomic		GRCh38 (hg38)	Primary Assembly		NC_000011.10	Chr11	46,386,979	46,387,139
nsv6032957	Remapped	Perfect	GRCh37.p13	Primary Assembly	First Pass	NC_000011.9	Chr11	46,408,529	46,408,689

Variant Call Information

Variant Call ID	Type	Method	Analysis
nssv17592921	deletion	Sequencing	Sequence alignment

Variant Call Placement Information

Variant Call ID	Placement Type	Score	HGVS	Assembly	Reciprocity	Sequence ID	Chr	Start	Stop
nssv17592921	Submitted genomic		NC_000011.10:g.463 86979_46387139del	GRCh38 (hg38)		NC_000011.10	Chr11	46,386,979	46,387,139
nssv17592921	Remapped	Perfect	NC_000011.9:g.4640 8529_46408689del	GRCh37.p13	First Pass	NC_000011.9	Chr11	46,408,529	46,408,689

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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