A curated catalogue of human genomic structural variation




Variant Details

Variant: essv25796359



Internal ID19160606
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr13:101554523..101650500hg38UCSC Ensembl
Innerchr13:102206874..102302850hg19UCSC Ensembl
Innerchr13:101004875..101100851hg18UCSC Ensembl
Cytoband13q33.1
Allele length
AssemblyAllele length
hg3895978
hg1995977
hg1895977
Variant TypeCNV loss
Copy Number1
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3892438
Supporting Variants
Samples
Known GenesITGBL1
MethodSNP array
Analysis
PlatformIllumina Human OmniExpress
CommentsNumber of probes=28
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)essv25796359
Frequency
Sample Size3017
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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