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dbVar

Database of genomic structural variation

nsv6752362

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:1,202

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: 135 SVs from 36 studies. See in: genome view

Submitted genomic67,487,069-67,488,270

Variant Region Placement Information

Variant Region ID	Placement Type	Score	Assembly	Assembly Unit	Reciprocity	Sequence ID	Chr	Start	Stop
nsv6752362	Submitted genomic		GRCh38 (hg38)	Primary Assembly		NC_000004.12	Chr4	67,487,069	67,488,270
nsv6752362	Remapped	Perfect	GRCh37.p13	Primary Assembly	First Pass	NC_000004.11	Chr4	68,352,787	68,353,988

Variant Call Information

Variant Call ID	Type	Method	Analysis
nssv18498656	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
nssv18498656	Submitted genomic		NC_000004.12:g.674 87069_67488270del	GRCh38 (hg38)		NC_000004.12	Chr4	67,487,069	67,488,270
nssv18498656	Remapped	Perfect	NC_000004.11:g.683 52787_68353988del	GRCh37.p13	First Pass	NC_000004.11	Chr4	68,352,787	68,353,988

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)
nssv18498656	0.008	1985	252354

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