A curated catalogue of human genomic structural variation




Variant Details

Variant: essv25797556



Internal ID18829951
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:31397531..31485862hg38UCSC Ensembl
Innerchr6:31365308..31453639hg19UCSC Ensembl
Innerchr6:31473287..31561618hg18UCSC Ensembl
Cytoband6p21.33
Allele length
AssemblyAllele length
hg3888332
hg1988332
hg1888332
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=150
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)essv25797556
Frequency
Sample Size3017
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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