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dbVar

Database of genomic structural variation

nsv6740221

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:3,258,304

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: 8036 SVs from 108 studies. See in: genome view

Submitted genomic71,124,425-74,382,728

Variant Region Placement Information

Variant Region ID	Placement Type	Score	Assembly	Assembly Unit	Reciprocity	Sequence ID	Chr	Start	Stop
nsv6740221	Submitted genomic		GRCh38 (hg38)	Primary Assembly		NC_000004.12	Chr4	71,124,425	74,382,728
nsv6740221	Remapped	Perfect	GRCh37.p13	Primary Assembly	First Pass	NC_000004.11	Chr4	71,990,142	75,248,445

Variant Call Information

Variant Call ID	Type	Method	Analysis
nssv18499453	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
nssv18499453	Submitted genomic		NC_000004.12:g.711 24425_74382728del	GRCh38 (hg38)		NC_000004.12	Chr4	71,124,425	74,382,728
nssv18499453	Remapped	Perfect	NC_000004.11:g.719 90142_75248445del	GRCh37.p13	First Pass	NC_000004.11	Chr4	71,990,142	75,248,445

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)
nssv18499453	4e-06	0	275172

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