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dbVar

Database of genomic structural variation

nsv6902995

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:649,838

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: 2460 SVs from 114 studies. See in: genome view

Submitted genomic4,619,101-5,268,938

Variant Region Placement Information

Variant Region ID	Placement Type	Score	Assembly	Assembly Unit	Reciprocity	Sequence ID	Chr	Start	Stop
nsv6902995	Submitted genomic		GRCh38 (hg38)	Primary Assembly		NC_000011.10	Chr11	4,619,101	5,268,938
nsv6902995	Remapped	Perfect	GRCh37.p13	Primary Assembly	First Pass	NC_000011.9	Chr11	4,640,331	5,290,168

Variant Call Information

Variant Call ID	Type	Method	Analysis
nssv18577828	duplication	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
nssv18577828	Submitted genomic		NC_000011.10:g.461 9101_5268938dup	GRCh38 (hg38)		NC_000011.10	Chr11	4,619,101	5,268,938
nssv18577828	Remapped	Perfect	NC_000011.9:g.4640 331_5290168dup	GRCh37.p13	First Pass	NC_000011.9	Chr11	4,640,331	5,290,168

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)
nssv18577828	3.6e-05	10	275428

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