A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv5951n100



Internal ID22792038
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:32655500..32713868hg38UCSC Ensembl
chr6:32623277..32681645hg19UCSC Ensembl
chr6:32731255..32789623hg18UCSC Ensembl
Cytoband6p21.32
Allele length
AssemblyAllele length
hg3858369
hg1958369
hg1858369
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1024857, nsv1024742
Samples
Known GenesHLA-DQB1
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)dgv5951n100
Frequency
Sample Size11257
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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