A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv694298



Internal ID15084264
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:93592687..93604195hg38UCSC Ensembl
Innerchr6:94302405..94313913hg19UCSC Ensembl
Innerchr6:94359126..94370634hg18UCSC Ensembl
Innerchr6:94359126..94370634hg17UCSC Ensembl
Cytoband6q16.1
Allele length
AssemblyAllele length
hg3811509
hg1911509
hg1811509
hg1711509
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv517329
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv694298
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