A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3892575



Internal ID18836709
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr14:90114643..90177668hg38UCSC Ensembl
Outerchr14:90114643..90177668hg38UCSC Ensembl
Innerchr14:90580987..90644012hg19UCSC Ensembl
Outerchr14:90580987..90644012hg19UCSC Ensembl
Innerchr14:89650740..89713765hg18UCSC Ensembl
Outerchr14:89650740..89713765hg18UCSC Ensembl
Cytoband14q32.11
Allele length
AssemblyAllele length
hg3863026
hg1963026
hg1863026
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv25792904
Samples
Known GenesKCNK13
MethodSNP array
Analysis
PlatformIllumina HumanHap 610
Comments
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)esv3892575
Frequency
Sample Size3017
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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