A curated catalogue of human genomic structural variation




Variant Details

Variant: essv25791388



Internal ID19161631
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr14:62167862..62276894hg38UCSC Ensembl
Innerchr14:62634580..62743612hg19UCSC Ensembl
Innerchr14:61704333..61813365hg18UCSC Ensembl
Cytoband14q23.2
Allele length
AssemblyAllele length
hg38109033
hg19109033
hg18109033
Variant TypeCNV gain
Copy Number3
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3892553
Supporting Variants
Samples
Known Genes
MethodSNP array
Analysis
PlatformIllumina HumanHap 610
CommentsNumber of probes=34
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)essv25791388
Frequency
Sample Size3017
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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