A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv573139



Internal ID16360548
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:78137842..78138355hg38UCSC Ensembl
Innerchr16:78171739..78172252hg19UCSC Ensembl
Innerchr16:76729240..76729753hg18UCSC Ensembl
Cytoband16q23.1
Allele length
AssemblyAllele length
hg38514
hg19514
hg18514
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv5217n54
Supporting Variantsnssv860926, nssv860929, nssv860927, nssv860928, nssv860931, nssv860930, nssv860925, nssv860924, nssv860932
Samples
Known GenesWWOX
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv573139
Frequency
Sample Size17421
Observed Gain0
Observed Loss9
Observed Complex0
Frequencyn/a


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