A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3892362



Internal ID19183182
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr13:59852121..59918371hg38UCSC Ensembl
Outerchr13:59818072..59978884hg38UCSC Ensembl
Innerchr13:60426255..60492505hg19UCSC Ensembl
Outerchr13:60392206..60553018hg19UCSC Ensembl
Innerchr13:59324256..59390506hg18UCSC Ensembl
Outerchr13:59290207..59451019hg18UCSC Ensembl
Cytoband13q21.2
Allele length
AssemblyAllele length
hg38160813
hg19160813
hg18160813
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv25784356, essv25798993
Samples
Known GenesDIAPH3
MethodSNP array
Analysis
PlatformIllumina HumanHap 610
Comments
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)esv3892362
Frequency
Sample Size3017
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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