A curated catalogue of human genomic structural variation




Variant Details

Variant: essv25790589



Internal ID19159780
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:45135514..45372115hg38UCSC Ensembl
Innerchr3:45177006..45413607hg19UCSC Ensembl
Innerchr3:45152010..45388611hg18UCSC Ensembl
Cytoband3p21.31
Allele length
AssemblyAllele length
hg38236602
hg19236602
hg18236602
Variant TypeCNV gain
Copy Number3
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3893691
Supporting Variants
Samples
Known GenesCDCP1, TMEM158
MethodSNP array
Analysis
PlatformIllumina HumanHap 610
CommentsNumber of probes=69
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)essv25790589
Frequency
Sample Size3017
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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