A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14098341



Internal ID21291085
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:83685844..83693686hg38UCSC Ensembl
Innerchr16:83719449..83727291hg19UCSC Ensembl
Cytoband16q23.3
Allele length
AssemblyAllele length
hg387843
hg197843
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3114770
Supporting Variants
Samplessample69
Known GenesCDH13
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nssv14098341
Frequency
Sample Size467
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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