A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17708395



Internal ID132061
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:86473525..86474784hg38UCSC Ensembl
chr16:86507131..86508390hg19UCSC Ensembl
Cytoband16q24.1
Allele length
AssemblyAllele length
hg381260
hg191260
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5518349
Supporting Variants
Samples
Known GenesFENDRR
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17708395
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.000312


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