A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv599952



Internal ID16040675
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr5:149851956..149881249hg38UCSC Ensembl
Innerchr5:149231519..149260812hg19UCSC Ensembl
Innerchr5:149211712..149241005hg18UCSC Ensembl
Cytoband5q32
Allele length
AssemblyAllele length
hg3829294
hg1929294
hg1829294
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv10112n54
Supporting Variantsnssv1153610
SamplesHGDP00155
Known GenesPDE6A, PPARGC1B
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv599952
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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