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dbVar

Database of genomic structural variation

nsv6693943

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:4,715

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: 127 SVs from 26 studies. See in: genome view

Submitted genomic134,385,923-134,390,637

Variant Region Placement Information

Variant Region ID	Placement Type	Score	Assembly	Assembly Unit	Reciprocity	Sequence ID	Chr	Start	Stop
nsv6693943	Submitted genomic		GRCh38 (hg38)	Primary Assembly		NC_000002.12	Chr2	134,385,923	134,390,637
nsv6693943	Remapped	Perfect	GRCh37.p13	Primary Assembly	First Pass	NC_000002.11	Chr2	135,143,494	135,148,208

Variant Call Information

Variant Call ID	Type	Method	Analysis
nssv18442587	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
nssv18442587	Submitted genomic		NC_000002.12:g.134 385923_134390637de l	GRCh38 (hg38)		NC_000002.12	Chr2	134,385,923	134,390,637
nssv18442587	Remapped	Perfect	NC_000002.11:g.135 143494_135148208de l	GRCh37.p13	First Pass	NC_000002.11	Chr2	135,143,494	135,148,208

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)
nssv18442587	1.8e-05	5	275058

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