A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1151326



Internal ID15526899
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr2:166170659..166216180hg38UCSC Ensembl
Innerchr2:167027169..167072690hg19UCSC Ensembl
Innerchr2:166735415..166780936hg18UCSC Ensembl
Cytoband2q24.3
Allele length
AssemblyAllele length
hg3845522
hg1945522
hg1845522
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv583585
Supporting Variants
SamplesHGDP00251
Known GenesSCN9A
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv1151326
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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