A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv6114n100



Internal ID22792201
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:102229496..102287407hg38UCSC Ensembl
chr6:102677371..102735282hg19UCSC Ensembl
chr6:102784064..102841975hg18UCSC Ensembl
Cytoband6q16.3
Allele length
AssemblyAllele length
hg3857912
hg1957912
hg1857912
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1019242, nsv1030970
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)dgv6114n100
Frequency
Sample Size11257
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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