A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17708284



Internal ID131950
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:74978018..74978135hg38UCSC Ensembl
chr16:75011916..75012033hg19UCSC Ensembl
Cytoband16q23.1
Allele length
AssemblyAllele length
hg38118
hg19118
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5531078
Supporting Variants
Samples
Known GenesWDR59
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17708284
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.000624


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