A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv852302



Internal ID15799572
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:4315234..4316393hg38UCSC Ensembl
Innerchr16:4365235..4366394hg19UCSC Ensembl
Innerchr16:4305236..4306395hg18UCSC Ensembl
Cytoband16p13.3
Allele length
AssemblyAllele length
hg381160
hg191160
hg181160
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv571275
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)nssv852302
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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