A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv573395



Internal ID16014118
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:83165860..83174417hg38UCSC Ensembl
Innerchr16:83199465..83208022hg19UCSC Ensembl
Innerchr16:81756966..81765523hg18UCSC Ensembl
Cytoband16q23.3
Allele length
AssemblyAllele length
hg388558
hg198558
hg188558
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv861982
Samples
Known GenesCDH13
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv573395
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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