A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17704622



Internal ID128288
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:11934227..11934784hg38UCSC Ensembl
chr16:12028084..12028641hg19UCSC Ensembl
Cytoband16p13.13
Allele length
AssemblyAllele length
hg38558
hg19558
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5532040
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17704622
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.000312


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