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dbVar

Database of genomic structural variation

nsv6716561

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:10,398

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: 213 SVs from 30 studies. See in: genome view

Submitted genomic237,631,679-237,642,076

Variant Region Placement Information

Variant Region ID	Placement Type	Score	Assembly	Assembly Unit	Reciprocity	Sequence ID	Chr	Start	Stop
nsv6716561	Submitted genomic		GRCh38 (hg38)	Primary Assembly		NC_000002.12	Chr2	237,631,679	237,642,076
nsv6716561	Remapped	Perfect	GRCh37.p13	Primary Assembly	First Pass	NC_000002.11	Chr2	238,540,322	238,550,719

Variant Call Information

Variant Call ID	Type	Method	Analysis
nssv18462144	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
nssv18462144	Submitted genomic		NC_000002.12:g.237 631679_237642076de l	GRCh38 (hg38)		NC_000002.12	Chr2	237,631,679	237,642,076
nssv18462144	Remapped	Perfect	NC_000002.11:g.238 540322_238550719de l	GRCh37.p13	First Pass	NC_000002.11	Chr2	238,540,322	238,550,719

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)
nssv18462144	4e-06	1	276186

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