A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv571291



Internal ID16358700
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:4315444..4316720hg38UCSC Ensembl
Innerchr16:4365445..4366721hg19UCSC Ensembl
Innerchr16:4305446..4306722hg18UCSC Ensembl
Cytoband16p13.3
Allele length
AssemblyAllele length
hg381277
hg191277
hg181277
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv4883n54
Supporting Variantsnssv852326
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv571291
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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