A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17709864



Internal ID133530
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:81709486..81709564hg38UCSC Ensembl
chr16:81743091..81743169hg19UCSC Ensembl
Cytoband16q23.3
Allele length
AssemblyAllele length
hg3879
hg1979
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5523815
Supporting Variants
Samples
Known GenesCMIP
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17709864
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.000156


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