A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17704965



Internal ID128631
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:10500452..10524602hg38UCSC Ensembl
chr16:10594309..10618459hg19UCSC Ensembl
Cytoband16p13.13
Allele length
AssemblyAllele length
hg3824151
hg1924151
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5528077
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17704965
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.000312


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