A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3892382



Internal ID19183202
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr13:68679730..68767854hg38UCSC Ensembl
Outerchr13:68679730..68767854hg38UCSC Ensembl
Innerchr13:69253862..69341986hg19UCSC Ensembl
Outerchr13:69253862..69341986hg19UCSC Ensembl
Innerchr13:68151863..68239987hg18UCSC Ensembl
Outerchr13:68151863..68239987hg18UCSC Ensembl
Cytoband13q21.33
Allele length
AssemblyAllele length
hg3888125
hg1988125
hg1888125
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv25789907
Samples
Known Genes
MethodSNP array
Analysis
PlatformIllumina HumanHap 610
Comments
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)esv3892382
Frequency
Sample Size3017
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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