A curated catalogue of human genomic structural variation




Variant Details

Variant: essv25788875



Internal ID19168373
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr14:42079252..42290902hg38UCSC Ensembl
Innerchr14:42548455..42760105hg19UCSC Ensembl
Innerchr14:41618205..41829855hg18UCSC Ensembl
Cytoband14q21.1
Allele length
AssemblyAllele length
hg38211651
hg19211651
hg18211651
Variant TypeCNV gain
Copy Number3
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3892516
Supporting Variants
Samples
Known Genes
MethodSNP array
Analysis
PlatformIllumina HumanHap 610
CommentsNumber of probes=32
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)essv25788875
Frequency
Sample Size3017
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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