A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3892312



Internal ID19183132
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr13:23908914..23916782hg38UCSC Ensembl
Outerchr13:23906636..23916782hg38UCSC Ensembl
Innerchr13:24483053..24490921hg19UCSC Ensembl
Outerchr13:24480775..24490921hg19UCSC Ensembl
Innerchr13:23381053..23388921hg18UCSC Ensembl
Outerchr13:23378775..23388921hg18UCSC Ensembl
Cytoband13q12.12
Allele length
AssemblyAllele length
hg3810147
hg1910147
hg1810147
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv25780680, essv25781888
Samples
Known GenesANKRD20A19P
MethodSNP array
Analysis
PlatformIllumina HumanHap 610
Comments
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)esv3892312
Frequency
Sample Size3017
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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