A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17709490



Internal ID133156
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:57773848..57773974hg38UCSC Ensembl
chr16:57807760..57807886hg19UCSC Ensembl
Cytoband16q21
Allele length
AssemblyAllele length
hg38127
hg19127
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5517310
Supporting Variants
Samples
Known GenesKIFC3
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17709490
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.000156


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