A curated catalogue of human genomic structural variation




Variant Details

Variant: essv25788998



Internal ID19166473
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr14:105601281..105721708hg38UCSC Ensembl
Innerchr14:106067618..106188045hg19UCSC Ensembl
Innerchr14:105138663..105259090hg18UCSC Ensembl
Cytoband14q32.33
Allele length
AssemblyAllele length
hg38120428
hg19120428
hg18120428
Variant TypeCNV gain
Copy Number3
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3892587
Supporting Variants
Samples
Known GenesELK2AP, MIR8071-1, MIR8071-2
MethodSNP array
Analysis
PlatformIllumina HumanHap 610
CommentsNumber of probes=15
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)essv25788998
Frequency
Sample Size3017
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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