A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv909354



Internal ID16203310
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr2:53029556..53067968hg38UCSC Ensembl
Innerchr2:53256694..53295106hg19UCSC Ensembl
Innerchr2:53110198..53148610hg18UCSC Ensembl
Cytoband2p16.2
Allele length
AssemblyAllele length
hg3838413
hg1938413
hg1838413
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv581982
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)nssv909354
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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