A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17709022



Internal ID132688
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:51818682..51829000hg38UCSC Ensembl
chr16:51852593..51862911hg19UCSC Ensembl
Cytoband16q12.1
Allele length
AssemblyAllele length
hg3810319
hg1910319
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5519504
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17709022
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.000156


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