A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17707431



Internal ID131097
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:52227882..52228708hg38UCSC Ensembl
chr16:52261794..52262620hg19UCSC Ensembl
Cytoband16q12.1
Allele length
AssemblyAllele length
hg38827
hg19827
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5516815
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17707431
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.000312


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