A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3892427



Internal ID19183247
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr13:93171161..93190146hg38UCSC Ensembl
Outerchr13:93164040..93206359hg38UCSC Ensembl
Innerchr13:93823414..93842399hg19UCSC Ensembl
Outerchr13:93816293..93858612hg19UCSC Ensembl
Innerchr13:92621415..92640400hg18UCSC Ensembl
Outerchr13:92614294..92656613hg18UCSC Ensembl
Cytoband13q31.3
Allele length
AssemblyAllele length
hg3842320
hg1942320
hg1842320
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv25789372, essv25792554, essv25790943
Samples
Known Genes
MethodSNP array
Analysis
PlatformIllumina HumanHap 610
Comments
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)esv3892427
Frequency
Sample Size3017
Observed Gain3
Observed Loss0
Observed Complex0
Frequencyn/a


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