A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv2883186



Internal ID15400912
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr2:32999421..33002119hg38UCSC Ensembl
Innerchr2:33224488..33227186hg19UCSC Ensembl
Innerchr2:33077992..33080690hg18UCSC Ensembl
Cytoband2p22.3
Allele length
AssemblyAllele length
hg382699
hg192699
hg182699
Variant TypeCNV loss
Copy Number1
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv514057
Supporting Variants
SamplesNA19154
Known GenesLTBP1
MethodOligo aCGH
AnalysisADM2 threshold = 5
PlatformAgilent Eichler Human CNP 180K v3.0
Comments
ReferenceCampbell_et_al_2011
Pubmed ID21397061
Accession Number(s)nssv2883186
Frequency
Sample Size2366
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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