A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv573367



Internal ID16014090
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:82106956..83007241hg38UCSC Ensembl
Innerchr16:82140561..83040846hg19UCSC Ensembl
Innerchr16:80698062..81598347hg18UCSC Ensembl
Cytoband16q23.3
Allele length
AssemblyAllele length
hg38900286
hg19900286
hg18900286
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv861943
Samples
Known GenesCDH13, MIR8058, MPHOSPH6
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv573367
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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