A curated catalogue of human genomic structural variation




Variant Details

Variant: essv25790190



Internal ID19177655
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:32543791..32597007hg38UCSC Ensembl
Innerchr6:32511568..32564784hg19UCSC Ensembl
Innerchr6:32619546..32672762hg18UCSC Ensembl
Cytoband6p21.32
Allele length
AssemblyAllele length
hg3853217
hg1953217
hg1853217
Variant TypeCNV gain
Copy Number3
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3890832
Supporting Variants
Samples
Known GenesHLA-DRB1, HLA-DRB6
MethodSNP array
Analysis
PlatformIllumina HumanHap 610
CommentsNumber of probes=40
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)essv25790190
Frequency
Sample Size3017
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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