A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv566232



Internal ID16353641
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr14:105474226..105475136hg38UCSC Ensembl
Innerchr14:105940563..105941473hg19UCSC Ensembl
Innerchr14:105011608..105012518hg18UCSC Ensembl
Cytoband14q32.33
Allele length
AssemblyAllele length
hg38911
hg19911
hg18911
Variant TypeCNV gain+loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv3992n54
Supporting Variantsnssv834858, nssv834855, nssv834852, nssv834854, nssv834857, nssv834860, nssv834862, nssv834853, nssv834851, nssv834850, nssv834856, nssv834861, nssv834859, nssv834863
Samples
Known GenesCRIP2
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv566232
Frequency
Sample Size17421
Observed Gain9
Observed Loss5
Observed Complex0
Frequencyn/a


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