A curated catalogue of human genomic structural variation




Variant Details

Variant: essv25780680



Internal ID19170638
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr13:23906636..23916782hg38UCSC Ensembl
Innerchr13:24480775..24490921hg19UCSC Ensembl
Innerchr13:23378775..23388921hg18UCSC Ensembl
Cytoband13q12.12
Allele length
AssemblyAllele length
hg3810147
hg1910147
hg1810147
Variant TypeCNV loss
Copy Number1
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3892312
Supporting Variants
Samples
Known GenesANKRD20A19P
MethodSNP array
Analysis
PlatformIllumina HumanHap 610
CommentsNumber of probes=8
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)essv25780680
Frequency
Sample Size3017
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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