A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3893691



Internal ID19184511
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:45135514..45372115hg38UCSC Ensembl
Outerchr3:45135514..45372115hg38UCSC Ensembl
Innerchr3:45177006..45413607hg19UCSC Ensembl
Outerchr3:45177006..45413607hg19UCSC Ensembl
Innerchr3:45152010..45388611hg18UCSC Ensembl
Outerchr3:45152010..45388611hg18UCSC Ensembl
Cytoband3p21.31
Allele length
AssemblyAllele length
hg38236602
hg19236602
hg18236602
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv25790589
Samples
Known GenesCDCP1, TMEM158
MethodSNP array
Analysis
PlatformIllumina HumanHap 610
Comments
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)esv3893691
Frequency
Sample Size3017
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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