A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17709667



Internal ID133333
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:83757752..83779801hg38UCSC Ensembl
chr16:83791357..83813406hg19UCSC Ensembl
Cytoband16q23.3
Allele length
AssemblyAllele length
hg3822050
hg1922050
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5524363
Supporting Variants
Samples
Known GenesCDH13
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17709667
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.000312


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