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dbVar

Database of genomic structural variation

nsv6410965

Organism: Homo sapiens

Study:nstd223 (Sedlazeck et al. 2020)
Variant Type:copy number variation
Method Type:Sequencing
Submitted on:GRCh38

Variant Calls:1
Validation:Not tested
Clinical Assertions: No
Region Size:92,279

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: 2749 SVs from 104 studies. See in: genome view

Submitted genomic31,251,595-31,343,873

Variant Region Placement Information

Variant Region ID	Placement Type	Score	Assembly	Assembly Unit	Reciprocity	Sequence ID	Chr	Start	Stop
nsv6410965	Submitted genomic		GRCh38 (hg38)	Primary Assembly		NC_000006.12	Chr6	31,251,595	31,343,873
nsv6410965	Remapped	Perfect	GRCh37.p13	Primary Assembly	First Pass	NC_000006.11	Chr6	31,219,372	31,311,650

Variant Call Information

Variant Call ID	Type	Method	Analysis
nssv18142066	deletion	Sequencing	Sequence alignment

Variant Call Placement Information

Variant Call ID	Placement Type	Score	HGVS	Assembly	Reciprocity	Sequence ID	Chr	Start	Stop
nssv18142066	Submitted genomic		NC_000006.12:g.312 51595_31343873del	GRCh38 (hg38)		NC_000006.12	Chr6	31,251,595	31,343,873
nssv18142066	Remapped	Perfect	NC_000006.11:g.312 19372_31311650del	GRCh37.p13	First Pass	NC_000006.11	Chr6	31,219,372	31,311,650

No validation data were submitted for this variant

No clinical assertion data were submitted for this variant

Complete genotype and/or allele frequency data for this study can be found on dbVar's FTP site.

Genotype Information

Variant Call ID	Allele Frequency (AF)	Allele Count (AC)	Allele Number (AN)
nssv18142066	0.005	178	34520

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