A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17704594



Internal ID128260
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:11675795..11675863hg38UCSC Ensembl
chr16:11769651..11769719hg19UCSC Ensembl
Cytoband16p13.13
Allele length
AssemblyAllele length
hg3869
hg1969
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5527263
Supporting Variants
Samples
Known GenesSNN
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17704594
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.000156


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