A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3892435



Internal ID18836569
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr13:100324308..100420688hg38UCSC Ensembl
Outerchr13:100324308..100420688hg38UCSC Ensembl
Innerchr13:100976562..101072942hg19UCSC Ensembl
Outerchr13:100976562..101072942hg19UCSC Ensembl
Innerchr13:99774563..99870943hg18UCSC Ensembl
Outerchr13:99774563..99870943hg18UCSC Ensembl
Cytoband13q32.3
Allele length
AssemblyAllele length
hg3896381
hg1996381
hg1896381
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv25797200
Samples
Known GenesPCCA
MethodSNP array
Analysis
PlatformIllumina Human OmniExpress
Comments
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)esv3892435
Frequency
Sample Size3017
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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