A curated catalogue of human genomic structural variation




Variant Details

Variant: essv25788527



Internal ID19177728
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr14:26985012..27042183hg38UCSC Ensembl
Innerchr14:27454218..27511389hg19UCSC Ensembl
Innerchr14:26524058..26581229hg18UCSC Ensembl
Cytoband14q12
Allele length
AssemblyAllele length
hg3857172
hg1957172
hg1857172
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=16
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)essv25788527
Frequency
Sample Size3017
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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