A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv573663



Internal ID16014386
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:88572446..88575424hg38UCSC Ensembl
Innerchr16:88638854..88641832hg19UCSC Ensembl
Innerchr16:87166355..87169333hg18UCSC Ensembl
Cytoband16q24.2
Allele length
AssemblyAllele length
hg382979
hg192979
hg182979
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv5309n54
Supporting Variantsnssv863015, nssv863011, nssv863013, nssv863012, nssv863014
Samples
Known GenesZC3H18
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv573663
Frequency
Sample Size17421
Observed Gain0
Observed Loss5
Observed Complex0
Frequencyn/a


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