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dbVar

Database of genomic structural variation

nsv6958459

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:800

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: 103 SVs from 28 studies. See in: genome view

Submitted genomic91,493,201-91,494,000

Variant Region Placement Information

Variant Region ID	Placement Type	Score	Assembly	Assembly Unit	Reciprocity	Sequence ID	Chr	Start	Stop
nsv6958459	Submitted genomic		GRCh38 (hg38)	Primary Assembly		NC_000014.9	Chr14	91,493,201	91,494,000
nsv6958459	Remapped	Perfect	GRCh37.p13	Primary Assembly	First Pass	NC_000014.8	Chr14	91,959,545	91,960,344

Variant Call Information

Variant Call ID	Type	Method	Analysis
nssv18392913	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
nssv18392913	Submitted genomic		NC_000014.9:g.9149 3201_91494000del	GRCh38 (hg38)		NC_000014.9	Chr14	91,493,201	91,494,000
nssv18392913	Remapped	Perfect	NC_000014.8:g.9195 9545_91960344del	GRCh37.p13	First Pass	NC_000014.8	Chr14	91,959,545	91,960,344

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)
nssv18392913	0.032	7882	250716

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