A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3892379



Internal ID19183199
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr13:67667812..68133578hg38UCSC Ensembl
Outerchr13:67667812..68133578hg38UCSC Ensembl
Innerchr13:68241944..68707710hg19UCSC Ensembl
Outerchr13:68241944..68707710hg19UCSC Ensembl
Innerchr13:67139945..67605711hg18UCSC Ensembl
Outerchr13:67139945..67605711hg18UCSC Ensembl
Cytoband13q21.32
Allele length
AssemblyAllele length
hg38465767
hg19465767
hg18465767
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv25791486
Samples
Known Genes
MethodSNP array
Analysis
PlatformIllumina HumanHap 610
Comments
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)esv3892379
Frequency
Sample Size3017
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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