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dbVar

Database of genomic structural variation

nsv6963263

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:179

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: 244 SVs from 27 studies. See in: genome view

Submitted genomic100,909,978-100,910,156

Variant Region Placement Information

Variant Region ID	Placement Type	Score	Assembly	Assembly Unit	Reciprocity	Sequence ID	Chr	Start	Stop
nsv6963263	Submitted genomic		GRCh38 (hg38)	Primary Assembly		NC_000015.10	Chr15	100,909,978	100,910,156
nsv6963263	Remapped	Perfect	GRCh37.p13	Primary Assembly	First Pass	NC_000015.9	Chr15	101,450,183	101,450,361

Variant Call Information

Variant Call ID	Type	Method	Analysis
nssv18614946	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
nssv18614946	Submitted genomic		NC_000015.10:g.100 909978_100910156du p	GRCh38 (hg38)		NC_000015.10	Chr15	100,909,978	100,910,156
nssv18614946	Remapped	Perfect	NC_000015.9:g.1014 50183_101450361dup	GRCh37.p13	First Pass	NC_000015.9	Chr15	101,450,183	101,450,361

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)
nssv18614946	2.7e-05	6	219118

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