A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3892390



Internal ID19183210
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr13:72544333..72556588hg38UCSC Ensembl
Outerchr13:72544333..72556588hg38UCSC Ensembl
Innerchr13:73118471..73130726hg19UCSC Ensembl
Outerchr13:73118471..73130726hg19UCSC Ensembl
Innerchr13:72016472..72028727hg18UCSC Ensembl
Outerchr13:72016472..72028727hg18UCSC Ensembl
Cytoband13q21.33
Allele length
AssemblyAllele length
hg3812256
hg1912256
hg1812256
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv25797984
Samples
Known Genes
MethodSNP array
Analysis
PlatformIllumina Human OmniExpress
Comments
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)esv3892390
Frequency
Sample Size3017
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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