A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3892485



Internal ID19183305
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr14:26985012..27042183hg38UCSC Ensembl
Outerchr14:26985012..27059034hg38UCSC Ensembl
Innerchr14:27454218..27511389hg19UCSC Ensembl
Outerchr14:27454218..27528240hg19UCSC Ensembl
Innerchr14:26524058..26581229hg18UCSC Ensembl
Outerchr14:26524058..26598080hg18UCSC Ensembl
Cytoband14q12
Allele length
AssemblyAllele length
hg3874023
hg1974023
hg1874023
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv25788538, essv25788749, essv25788527
Samples
Known Genes
MethodSNP array
Analysis
PlatformIllumina HumanHap 610
Comments
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)esv3892485
Frequency
Sample Size3017
Observed Gain3
Observed Loss0
Observed Complex0
Frequencyn/a


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