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dbVar

Database of genomic structural variation

nsv5583922

Organism: Homo sapiens

Study:nstd207 (Ebert 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:54

Publication(s):Ebert 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: 805 SVs from 66 studies. See in: genome view

Submitted genomic168,078,580-168,078,633

Variant Region Placement Information

Variant Region ID	Placement Type	Score	Assembly	Assembly Unit	Reciprocity	Sequence ID	Chr	Start	Stop
nsv5583922	Submitted genomic		GRCh38 (hg38)	Primary Assembly		NC_000006.12	Chr6	168,078,580	168,078,633
nsv5583922	Remapped	Perfect	GRCh37.p13	Primary Assembly	First Pass	NC_000006.11	Chr6	168,479,260	168,479,313

Variant Call Information

Variant Call ID	Type	Sample ID	Method	Analysis	Other Calls in this Sample and Study
nssv17140525	deletion	HG02011	Sequencing	Sequence alignment	2,906

Variant Call Placement Information

Variant Call ID	Placement Type	Score	HGVS	Assembly	Reciprocity	Sequence ID	Chr	Start	Stop
nssv17140525	Submitted genomic		NC_000006.12:g.168 078580_168078633de lC	GRCh38 (hg38)		NC_000006.12	Chr6	168,078,580	168,078,633
nssv17140525	Remapped	Perfect	NC_000006.11:g.168 479260_168479313de lC	GRCh37.p13	First Pass	NC_000006.11	Chr6	168,479,260	168,479,313

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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