A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17708910



Internal ID132576
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:89829649..89831982hg38UCSC Ensembl
chr16:89896057..89898390hg19UCSC Ensembl
Cytoband16q24.3
Allele length
AssemblyAllele length
hg382334
hg192334
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5521693
Supporting Variants
Samples
Known GenesSPIRE2
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17708910
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.025913


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