A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3890831



Internal ID19185133
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:32487705..32562421hg38UCSC Ensembl
Outerchr6:32487705..32572441hg38UCSC Ensembl
Innerchr6:32455482..32530198hg19UCSC Ensembl
Outerchr6:32455482..32540218hg19UCSC Ensembl
Innerchr6:32563460..32638176hg18UCSC Ensembl
Outerchr6:32563460..32648196hg18UCSC Ensembl
Cytoband6p21.32
Allele length
AssemblyAllele length
hg3884737
hg1984737
hg1884737
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv25792000, essv25790942, essv25791443, essv25791824, essv25790593, essv25790626, essv25790095, essv25790134
Samples
Known GenesHLA-DRB5, HLA-DRB6
MethodSNP array
Analysis
PlatformIllumina HumanHap 610
Comments
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)esv3890831
Frequency
Sample Size3017
Observed Gain8
Observed Loss0
Observed Complex0
Frequencyn/a


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