A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv6024n100



Internal ID22792111
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:78134882..78336932hg38UCSC Ensembl
chr6:78844599..79046649hg19UCSC Ensembl
chr6:78901318..79103368hg18UCSC Ensembl
Cytoband6q14.1
Allele length
AssemblyAllele length
hg38202051
hg19202051
hg18202051
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1024073, nsv1023415, nsv1023790, nsv1034850, nsv1017442, nsv1022144, nsv1031493, nsv1032647, nsv1034723, nsv1027969, nsv1031420, nsv1032022, nsv1016124, nsv1018051
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)dgv6024n100
Frequency
Sample Size11257
Observed Gain24
Observed Loss0
Observed Complex0
Frequencyn/a


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