A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3892305



Internal ID19183125
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr13:20872906..20913460hg38UCSC Ensembl
Outerchr13:20872906..20913460hg38UCSC Ensembl
Innerchr13:21447045..21487599hg19UCSC Ensembl
Outerchr13:21447045..21487599hg19UCSC Ensembl
Innerchr13:20345045..20385599hg18UCSC Ensembl
Outerchr13:20345045..20385599hg18UCSC Ensembl
Cytoband13q12.11
Allele length
AssemblyAllele length
hg3840555
hg1940555
hg1840555
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv25798109
Samples
Known GenesXPO4
MethodSNP array
Analysis
PlatformIllumina Human OmniExpress
Comments
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)esv3892305
Frequency
Sample Size3017
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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