A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3890835



Internal ID19185137
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:32537754..32562421hg38UCSC Ensembl
Outerchr6:32537754..32575763hg38UCSC Ensembl
Innerchr6:32505531..32530198hg19UCSC Ensembl
Outerchr6:32505531..32543540hg19UCSC Ensembl
Innerchr6:32613509..32638176hg18UCSC Ensembl
Outerchr6:32613509..32651518hg18UCSC Ensembl
Cytoband6p21.32
Allele length
AssemblyAllele length
hg3838010
hg1938010
hg1838010
Variant TypeCNV gain+loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv25787583, essv25792194, essv25790000
Samples
Known GenesHLA-DRB6
MethodSNP array
Analysis
PlatformIllumina HumanHap 610
Comments
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)esv3890835
Frequency
Sample Size3017
Observed Gain2
Observed Loss1
Observed Complex0
Frequencyn/a


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