A curated catalogue of human genomic structural variation




Variant Details

Variant: essv25790127



Internal ID18820736
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr14:105721708..106207924hg38UCSC Ensembl
Innerchr14:106188045..106664567hg19UCSC Ensembl
Innerchr14:105259090..105735612hg18UCSC Ensembl
Cytoband14q32.33
Allele length
AssemblyAllele length
hg38486217
hg19476523
hg18476523
Variant TypeCNV gain
Copy Number3
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3892584
Supporting Variants
Samples
Known GenesADAM6, KIAA0125
MethodSNP array
Analysis
PlatformIllumina HumanHap 610
CommentsNumber of probes=30
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)essv25790127
Frequency
Sample Size3017
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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