A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv908395



Internal ID16202351
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr2:51052256..51169863hg38UCSC Ensembl
Innerchr2:51279394..51397001hg19UCSC Ensembl
Innerchr2:51132898..51250505hg18UCSC Ensembl
Cytoband2p16.3
Allele length
AssemblyAllele length
hg38117608
hg19117608
hg18117608
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv581867
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv908395
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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