A curated catalogue of human genomic structural variation




Variant Details

Variant: esv1006913



Internal ID6719028
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:33064893..33088398hg38UCSC Ensembl
Innerchr6:33032670..33056175hg19UCSC Ensembl
Innerchr6:33140648..33164153hg18UCSC Ensembl
Cytoband6p21.32
Allele length
AssemblyAllele length
hg3823506
hg1923506
hg1823506
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv3586721
SamplesHuRef
Known GenesHLA-DPA1, HLA-DPB1
MethodOligo aCGH
Analysis
PlatformNot Submitted
Comments
ReferencePang_et_al_2010
Pubmed ID20482838
Accession Number(s)esv1006913
Frequency
Sample Size3
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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