A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv6209n100



Internal ID22792296
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:170556631..170673434hg38UCSC Ensembl
chr6:170865719..170982522hg19UCSC Ensembl
chr6:170707644..170824447hg18UCSC Ensembl
Cytoband6q27
Allele length
AssemblyAllele length
hg38116804
hg19116804
hg18116804
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1030566, nsv1030193, nsv1029410, nsv1023735
Samples
Known GenesPDCD2, TBP
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)dgv6209n100
Frequency
Sample Size11257
Observed Gain6
Observed Loss0
Observed Complex0
Frequencyn/a


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