A curated catalogue of human genomic structural variation




Variant Details

Variant: essv25779910



Internal ID19182386
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr20:54852568..54880600hg38UCSC Ensembl
Innerchr20:53469107..53497139hg19UCSC Ensembl
Innerchr20:52902514..52930546hg18UCSC Ensembl
Cytoband20q13.2
Allele length
AssemblyAllele length
hg3828033
hg1928033
hg1828033
Variant TypeCNV loss
Copy Number1
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3893349
Supporting Variants
Samples
Known Genes
MethodSNP array
Analysis
PlatformIllumina HumanHap 610
CommentsNumber of probes=10
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)essv25779910
Frequency
Sample Size3017
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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