A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1150548



Internal ID15531759
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:15886390..15911711hg38UCSC Ensembl
Innerchr16:15980247..16005568hg19UCSC Ensembl
Innerchr16:15887748..15913069hg18UCSC Ensembl
Cytoband16p13.11
Allele length
AssemblyAllele length
hg3825322
hg1925322
hg1825322
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv571543
Supporting Variants
SamplesHGDP01202
Known GenesFOPNL
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv1150548
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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