A curated catalogue of human genomic structural variation




Variant Details

Variant: essv25798658



Internal ID18816468
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:31389614..31485841hg38UCSC Ensembl
Innerchr6:31357391..31453618hg19UCSC Ensembl
Innerchr6:31465370..31561597hg18UCSC Ensembl
Cytoband6p21.33
Allele length
AssemblyAllele length
hg3896228
hg1996228
hg1896228
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=169
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)essv25798658
Frequency
Sample Size3017
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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