A curated catalogue of human genomic structural variation




Variant Details

Variant: essv25796375



Internal ID19165659
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr20:4037932..4098576hg38UCSC Ensembl
Innerchr20:4018579..4079223hg19UCSC Ensembl
Innerchr20:3966579..4027223hg18UCSC Ensembl
Cytoband20p13
Allele length
AssemblyAllele length
hg3860645
hg1960645
hg1860645
Variant TypeCNV loss
Copy Number1
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3893271
Supporting Variants
Samples
Known Genes
MethodSNP array
Analysis
PlatformIllumina Human OmniExpress
CommentsNumber of probes=30
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)essv25796375
Frequency
Sample Size3017
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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