A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3666979



Internal ID18965260
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:12879480..12913681hg38UCSC Ensembl
Innerchr8:12736989..12771190hg19UCSC Ensembl
Innerchr8:12781360..12815561hg18UCSC Ensembl
Cytoband8p22
Allele length
AssemblyAllele length
hg3834202
hg1934202
hg1834202
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1033033
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)nssv3666979
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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