A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3892311



Internal ID18836445
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr13:23397028..24290919hg38UCSC Ensembl
Outerchr13:22674660..24411768hg38UCSC Ensembl
Innerchr13:23971167..24865057hg19UCSC Ensembl
Outerchr13:23248799..24985906hg19UCSC Ensembl
Innerchr13:22869167..23763057hg18UCSC Ensembl
Outerchr13:22146799..23883906hg18UCSC Ensembl
Cytoband13q12.11
Allele length
AssemblyAllele length
hg381737109
hg191737108
hg181737108
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv25789253, essv25792600, essv25791550
Samples
Known GenesANKRD20A19P, BASP1P1, C1QTNF9, C1QTNF9B, C1QTNF9B-AS1, LINC00327, MIPEP, MIR2276, SACS, SACS-AS1, SGCG, SPATA13, SPATA13-AS1, TNFRSF19
MethodSNP array
Analysis
PlatformIllumina HumanHap 610
Comments
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)esv3892311
Frequency
Sample Size3017
Observed Gain3
Observed Loss0
Observed Complex0
Frequencyn/a


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