A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv4926n54



Internal ID18997102
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:15883875..15924732hg38UCSC Ensembl
chr16:15977732..16018589hg19UCSC Ensembl
chr16:15885233..15926090hg18UCSC Ensembl
Cytoband16p13.11
Allele length
AssemblyAllele length
hg3840858
hg1940858
hg1840858
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv571544, nsv571542
SamplesHGDP00911, HGDP01201, HGDP00906, HGDP00907, HGDP00928, HGDP00941
Known GenesFOPNL
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)dgv4926n54
Frequency
Sample Size17421
Observed Gain7
Observed Loss0
Observed Complex0
Frequencyn/a


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