A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17707497



Internal ID131163
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:67374520..67377457hg38UCSC Ensembl
chr16:67408423..67411360hg19UCSC Ensembl
Cytoband16q22.1
Allele length
AssemblyAllele length
hg382938
hg192938
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5522079
Supporting Variants
Samples
Known GenesLRRC36
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17707497
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.000156


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