A curated catalogue of human genomic structural variation




Variant Details

Variant: essv25797200



Internal ID18832502
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr13:100324308..100420688hg38UCSC Ensembl
Innerchr13:100976562..101072942hg19UCSC Ensembl
Innerchr13:99774563..99870943hg18UCSC Ensembl
Cytoband13q32.3
Allele length
AssemblyAllele length
hg3896381
hg1996381
hg1896381
Variant TypeCNV loss
Copy Number1
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3892435
Supporting Variants
Samples
Known GenesPCCA
MethodSNP array
Analysis
PlatformIllumina Human OmniExpress
CommentsNumber of probes=19
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)essv25797200
Frequency
Sample Size3017
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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