A curated catalogue of human genomic structural variation




Variant Details

Variant: essv25782297



Internal ID18815492
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:31397622..31483790hg38UCSC Ensembl
Innerchr6:31365399..31451567hg19UCSC Ensembl
Innerchr6:31473378..31559546hg18UCSC Ensembl
Cytoband6p21.33
Allele length
AssemblyAllele length
hg3886169
hg1986169
hg1886169
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 HumanHap 610
CommentsNumber of probes=152
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)essv25782297
Frequency
Sample Size3017
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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