A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv573371



Internal ID16014094
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:82131578..83629456hg38UCSC Ensembl
Innerchr16:82165183..83663061hg19UCSC Ensembl
Innerchr16:80722684..82220562hg18UCSC Ensembl
Cytoband16q23.3
Allele length
AssemblyAllele length
hg381497879
hg191497879
hg181497879
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv861947
Samples
Known GenesCDH13, MIR3182, MIR8058, MPHOSPH6
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv573371
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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