A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17707033



Internal ID130699
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:61616547..61632886hg38UCSC Ensembl
chr16:61650451..61666790hg19UCSC Ensembl
Cytoband16q21
Allele length
AssemblyAllele length
hg3816340
hg1916340
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5520897
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17707033
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.000312


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