A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv573808



Internal ID16014531
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:89852442..89852908hg38UCSC Ensembl
Innerchr16:89918850..89919316hg19UCSC Ensembl
Innerchr16:88446351..88446817hg18UCSC Ensembl
Cytoband16q24.3
Allele length
AssemblyAllele length
hg38467
hg19467
hg18467
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv5335n54
Supporting Variantsnssv863684, nssv863682, nssv863687, nssv863683, nssv863685, nssv863686
Samples
Known GenesSPIRE2
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv573808
Frequency
Sample Size17421
Observed Gain0
Observed Loss6
Observed Complex0
Frequencyn/a


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