A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3892480



Internal ID19183300
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr14:25053805..25274278hg38UCSC Ensembl
Outerchr14:25053805..25274278hg38UCSC Ensembl
Innerchr14:25523011..25743484hg19UCSC Ensembl
Outerchr14:25523011..25743484hg19UCSC Ensembl
Innerchr14:24592851..24813324hg18UCSC Ensembl
Outerchr14:24592851..24813324hg18UCSC Ensembl
Cytoband14q12
Allele length
AssemblyAllele length
hg38220474
hg19220474
hg18220474
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv25790548
Samples
Known Genes
MethodSNP array
Analysis
PlatformIllumina HumanHap 610
Comments
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)esv3892480
Frequency
Sample Size3017
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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