A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3890832



Internal ID19185134
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:32543791..32588753hg38UCSC Ensembl
Outerchr6:32531057..32597007hg38UCSC Ensembl
Innerchr6:32511568..32556530hg19UCSC Ensembl
Outerchr6:32498834..32564784hg19UCSC Ensembl
Innerchr6:32619546..32664508hg18UCSC Ensembl
Outerchr6:32606812..32672762hg18UCSC Ensembl
Cytoband6p21.32
Allele length
AssemblyAllele length
hg3865951
hg1965951
hg1865951
Variant TypeCNV gain+loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv25790190, essv25797235, essv25797145
Samples
Known GenesHLA-DRB1, HLA-DRB6
MethodSNP array
Analysis
PlatformIllumina HumanHap 610
Illumina Human OmniExpress
Comments
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)esv3890832
Frequency
Sample Size3017
Observed Gain1
Observed Loss2
Observed Complex0
Frequencyn/a


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