A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17708012



Internal ID131678
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:23698712..23698828hg38UCSC Ensembl
chr16:23710033..23710149hg19UCSC Ensembl
Cytoband16p12.2
Allele length
AssemblyAllele length
hg38117
hg19117
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5522859
Supporting Variants
Samples
Known GenesERN2
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17708012
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.002966


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