A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17708010



Internal ID131676
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:23665976..23666052hg38UCSC Ensembl
chr16:23677297..23677373hg19UCSC Ensembl
Cytoband16p12.2
Allele length
AssemblyAllele length
hg3877
hg1977
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5527415
Supporting Variants
Samples
Known GenesDCTN5
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17708010
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.000624


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