A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv671816



Internal ID15408468
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:155359727..155376740hg38UCSC Ensembl
Innerchr6:155680861..155697874hg19UCSC Ensembl
Innerchr6:155722553..155739566hg18UCSC Ensembl
Innerchr6:155772974..155789987hg17UCSC Ensembl
Cytoband6q25.3
Allele length
AssemblyAllele length
hg3817014
hg1917014
hg1817014
hg1717014
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv520490
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv671816
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer