A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3659042



Internal ID18957323
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:76730151..76758909hg38UCSC Ensembl
Innerchr6:77439868..77468626hg19UCSC Ensembl
Innerchr6:77496587..77525345hg18UCSC Ensembl
Cytoband6q14.1
Allele length
AssemblyAllele length
hg3828759
hg1928759
hg1828759
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1031654
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3659042
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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