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

dbVar

Database of genomic structural variation

nsv6751490

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:8,816

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: 145 SVs from 33 studies. See in: genome view

Submitted genomic141,668,528-141,677,343

Variant Region Placement Information

Variant Region ID	Placement Type	Score	Assembly	Assembly Unit	Reciprocity	Sequence ID	Chr	Start	Stop
nsv6751490	Submitted genomic		GRCh38 (hg38)	Primary Assembly		NC_000004.12	Chr4	141,668,528	141,677,343
nsv6751490	Remapped	Perfect	GRCh37.p13	Primary Assembly	First Pass	NC_000004.11	Chr4	142,589,681	142,598,496

Variant Call Information

Variant Call ID	Type	Method	Analysis
nssv18685221	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
nssv18685221	Submitted genomic		NC_000004.12:g.141 668528_141677343du p	GRCh38 (hg38)		NC_000004.12	Chr4	141,668,528	141,677,343
nssv18685221	Remapped	Perfect	NC_000004.11:g.142 589681_142598496du p	GRCh37.p13	First Pass	NC_000004.11	Chr4	142,589,681	142,598,496

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)
nssv18685221	4e-06	1	275804

You are here: NCBI