A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17708332



Internal ID131998
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:84569094..84602270hg38UCSC Ensembl
chr16:84602700..84635876hg19UCSC Ensembl
Cytoband16q24.1
Allele length
AssemblyAllele length
hg3833177
hg1933177
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5520056
Supporting Variants
Samples
Known GenesCOTL1
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17708332
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.000156


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