A curated catalogue of human genomic structural variation




Variant Details

Variant: essv25788538



Internal ID19178490
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr14:26985012..27050905hg38UCSC Ensembl
Innerchr14:27454218..27520111hg19UCSC Ensembl
Innerchr14:26524058..26589951hg18UCSC Ensembl
Cytoband14q12
Allele length
AssemblyAllele length
hg3865894
hg1965894
hg1865894
Variant TypeCNV gain
Copy Number3
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3892485
Supporting Variants
Samples
Known Genes
MethodSNP array
Analysis
PlatformIllumina HumanHap 610
CommentsNumber of probes=17
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)essv25788538
Frequency
Sample Size3017
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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