A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1020665



Internal ID19109884
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:94187074..94219834hg38UCSC Ensembl
Innerchr8:95199302..95232062hg19UCSC Ensembl
Innerchr8:95268478..95301238hg18UCSC Ensembl
Cytoband8q22.1
Allele length
AssemblyAllele length
hg3832761
hg1932761
hg1832761
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3757323
Samples
Known GenesCDH17
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1020665
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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