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dbVar

Database of genomic structural variation

nsv6984968

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:13,612

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: 324 SVs from 45 studies. See in: genome view

Submitted genomic17,701,483-17,715,094

Variant Region Placement Information

Variant Region ID	Placement Type	Score	Assembly	Assembly Unit	Reciprocity	Sequence ID	Chr	Start	Stop
nsv6984968	Submitted genomic		GRCh38 (hg38)	Primary Assembly		NC_000017.11	Chr17	17,701,483	17,715,094
nsv6984968	Remapped	Perfect	GRCh37.p13	Primary Assembly	First Pass	NC_000017.10	Chr17	17,604,797	17,618,408

Variant Call Information

Variant Call ID	Type	Method	Analysis
nssv18407414	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
nssv18407414	Submitted genomic		NC_000017.11:g.177 01483_17715094del	GRCh38 (hg38)		NC_000017.11	Chr17	17,701,483	17,715,094
nssv18407414	Remapped	Perfect	NC_000017.10:g.176 04797_17618408del	GRCh37.p13	First Pass	NC_000017.10	Chr17	17,604,797	17,618,408

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)
nssv18407414	1.1e-05	3	275936

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