A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv514152



Internal ID15465846
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:62727469..62729805hg38UCSC Ensembl
Innerchr3:62713144..62715480hg19UCSC Ensembl
Innerchr3:62688184..62690520hg18UCSC Ensembl
Cytoband3p14.2
Allele length
AssemblyAllele length
hg382337
hg192337
hg182337
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2899056, nssv2899057, nssv2899050, nssv2899054, nssv2899063, nssv2899058, nssv2899053, nssv2899052, nssv2899049, nssv2899064, nssv2899055, nssv2899061, nssv2899060, nssv2899051, nssv2899062, nssv2899059
SamplesNA18870, NA19252, NA18501, NA18500, NA18516, NA18489, NA19144, NA19210, NA19199, NA19145, NA18907, NA18872, NA19128, NA19160, NA19198, NA18908
Known GenesCADPS
MethodOligo aCGH
AnalysisADM2 threshold = 5
PlatformAgilent Eichler Human CNP 180K v3.0
Comments
ReferenceCampbell_et_al_2011
Pubmed ID21397061
Accession Number(s)nsv514152
Frequency
Sample Size2366
Observed Gain0
Observed Loss16
Observed Complex0
Frequencyn/a


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