A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1150551



Internal ID15530362
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:15886390..15924732hg38UCSC Ensembl
Innerchr16:15980247..16018589hg19UCSC Ensembl
Innerchr16:15887748..15926090hg18UCSC Ensembl
Cytoband16p13.11
Allele length
AssemblyAllele length
hg3838343
hg1938343
hg1838343
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv571544
Supporting Variants
SamplesHGDP00928
Known GenesFOPNL
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv1150551
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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