A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3890834



Internal ID19185136
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:32533938..32551227hg38UCSC Ensembl
Outerchr6:32528971..32553474hg38UCSC Ensembl
Innerchr6:32501715..32519004hg19UCSC Ensembl
Outerchr6:32496748..32521251hg19UCSC Ensembl
Innerchr6:32609693..32626982hg18UCSC Ensembl
Outerchr6:32604726..32629229hg18UCSC Ensembl
Cytoband6p21.32
Allele length
AssemblyAllele length
hg3824504
hg1924504
hg1824504
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv25796197, essv25798995, essv25785720
Samples
Known GenesHLA-DRB5, HLA-DRB6
MethodSNP array
Analysis
PlatformIllumina HumanHap 610
Illumina Human OmniExpress
Comments
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)esv3890834
Frequency
Sample Size3017
Observed Gain0
Observed Loss3
Observed Complex0
Frequencyn/a


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