A curated catalogue of human genomic structural variation




Variant Details

Variant: essv25796713



Internal ID19163375
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr13:100161230..100371219hg38UCSC Ensembl
Innerchr13:100813484..101023473hg19UCSC Ensembl
Innerchr13:99611485..99821474hg18UCSC Ensembl
Cytoband13q32.3
Allele length
AssemblyAllele length
hg38209990
hg19209990
hg18209990
Variant TypeCNV loss
Copy Number1
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3892434
Supporting Variants
Samples
Known GenesPCCA
MethodSNP array
Analysis
PlatformIllumina Human OmniExpress
CommentsNumber of probes=24
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)essv25796713
Frequency
Sample Size3017
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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