A curated catalogue of human genomic structural variation




Variant Details

Variant: essv25792190



Internal ID18828192
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr14:105721708..106115912hg38UCSC Ensembl
Innerchr14:106188045..106572510hg19UCSC Ensembl
Innerchr14:105259090..105643555hg18UCSC Ensembl
Cytoband14q32.33
Allele length
AssemblyAllele length
hg38394205
hg19384466
hg18384466
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=21
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)essv25792190
Frequency
Sample Size3017
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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