A curated catalogue of human genomic structural variation




Variant Details

Variant: essv25797544



Internal ID18831181
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:31392478..31486587hg38UCSC Ensembl
Innerchr6:31360255..31454364hg19UCSC Ensembl
Innerchr6:31468234..31562343hg18UCSC Ensembl
Cytoband6p21.33
Allele length
AssemblyAllele length
hg3894110
hg1994110
hg1894110
Variant TypeCNV loss
Copy Number1
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3890819
Supporting Variants
Samples
Known GenesHCG26, HCP5, MICA
MethodSNP array
Analysis
PlatformIllumina Human OmniExpress
CommentsNumber of probes=161
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)essv25797544
Frequency
Sample Size3017
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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