A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17709105



Internal ID132771
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:66605434..66605541hg38UCSC Ensembl
chr16:66639337..66639444hg19UCSC Ensembl
Cytoband16q21
Allele length
AssemblyAllele length
hg38108
hg19108
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5515731
Supporting Variants
Samples
Known GenesCMTM3
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17709105
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.000312


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer