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dbVar

Database of genomic structural variation

nsv6834088

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:2,900

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

Submitted genomic105,069,117-105,072,016

Variant Region Placement Information

Variant Region ID	Placement Type	Score	Assembly	Assembly Unit	Reciprocity	Sequence ID	Chr	Start	Stop
nsv6834088	Submitted genomic		GRCh38 (hg38)	Primary Assembly		NC_000007.14	Chr7	105,069,117	105,072,016
nsv6834088	Remapped	Perfect	GRCh37.p13	Primary Assembly	First Pass	NC_000007.13	Chr7	104,709,564	104,712,463

Variant Call Information

Variant Call ID	Type	Method	Analysis
nssv18531926	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
nssv18531926	Submitted genomic		NC_000007.14:g.105 069117_105072016de l	GRCh38 (hg38)		NC_000007.14	Chr7	105,069,117	105,072,016
nssv18531926	Remapped	Perfect	NC_000007.13:g.104 709564_104712463de l	GRCh37.p13	First Pass	NC_000007.13	Chr7	104,709,564	104,712,463

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)
nssv18531926	4e-06	1	272142

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