A curated catalogue of human genomic structural variation




Variant Details

Variant: essv25798109



Internal ID19167257
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr13:20872906..20913460hg38UCSC Ensembl
Innerchr13:21447045..21487599hg19UCSC Ensembl
Innerchr13:20345045..20385599hg18UCSC Ensembl
Cytoband13q12.11
Allele length
AssemblyAllele length
hg3840555
hg1940555
hg1840555
Variant TypeCNV loss
Copy Number1
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3892305
Supporting Variants
Samples
Known GenesXPO4
MethodSNP array
Analysis
PlatformIllumina Human OmniExpress
CommentsNumber of probes=7
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)essv25798109
Frequency
Sample Size3017
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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