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dbVar

Database of genomic structural variation

nsv7024644

Organism: Homo sapiens

Study:nstd229 (Jun et al. 2023)
Variant Type:copy number variation
Method Type:Sequencing
Submitted on:GRCh38

Variant Calls:1
Validation:Not tested
Clinical Assertions: No
Region Size:12,812

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: 376 SVs from 30 studies. See in: genome view

Submitted genomic49,834,475-49,847,286

Variant Region Placement Information

Variant Region ID	Placement Type	Score	Assembly	Assembly Unit	Reciprocity	Sequence ID	Chr	Start	Stop
nsv7024644	Submitted genomic		GRCh38 (hg38)	Primary Assembly		NC_000022.11	Chr22	49,834,475	49,847,286
nsv7024644	Remapped	Perfect	GRCh37.p13	Primary Assembly	First Pass	NC_000022.10	Chr22	50,228,123	50,240,934

Variant Call Information

Variant Call ID	Type	Method	Analysis
nssv18457035	deletion	Sequencing	Split read and paired-end mapping

Variant Call Placement Information

Variant Call ID	Placement Type	Score	HGVS	Assembly	Reciprocity	Sequence ID	Chr	Start	Stop
nssv18457035	Submitted genomic		NC_000022.11:g.498 34475_49847286del	GRCh38 (hg38)		NC_000022.11	Chr22	49,834,475	49,847,286
nssv18457035	Remapped	Perfect	NC_000022.10:g.502 28123_50240934del	GRCh37.p13	First Pass	NC_000022.10	Chr22	50,228,123	50,240,934

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)
nssv18457035	7e-06	2	276178

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