A curated catalogue of human genomic structural variation




Variant Details

Variant: essv25780182



Internal ID19182691
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr20:23691103..23750857hg38UCSC Ensembl
Innerchr20:23671740..23731494hg19UCSC Ensembl
Innerchr20:23619740..23679494hg18UCSC Ensembl
Cytoband20p11.21
Allele length
AssemblyAllele length
hg3859755
hg1959755
hg1859755
Variant TypeCNV loss
Copy Number1
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3893321
Supporting Variants
Samples
Known GenesCST1
MethodSNP array
Analysis
PlatformIllumina HumanHap 610
CommentsNumber of probes=17
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)essv25780182
Frequency
Sample Size3017
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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