Warning: The NCBI web site requires JavaScript to function. more...

dbVar

Database of genomic structural variation

nsv6869399

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:7,465

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: 146 SVs from 29 studies. See in: genome view

Submitted genomic130,729,682-130,737,146

Variant Region Placement Information

Variant Region ID	Placement Type	Score	Assembly	Assembly Unit	Reciprocity	Sequence ID	Chr	Start	Stop
nsv6869399	Submitted genomic		GRCh38 (hg38)	Primary Assembly		NC_000009.12	Chr9	130,729,682	130,737,146
nsv6869399	Remapped	Perfect	GRCh37.p13	Primary Assembly	First Pass	NC_000009.11	Chr9	133,605,069	133,612,533

Variant Call Information

Variant Call ID	Type	Method	Analysis
nssv18565726	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
nssv18565726	Submitted genomic		NC_000009.12:g.130 729682_130737146de l	GRCh38 (hg38)		NC_000009.12	Chr9	130,729,682	130,737,146
nssv18565726	Remapped	Perfect	NC_000009.11:g.133 605069_133612533de l	GRCh37.p13	First Pass	NC_000009.11	Chr9	133,605,069	133,612,533

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)
nssv18565726	7.5e-05	21	275886

You are here: NCBI