A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16909238



Internal ID6947
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:17616501..17616711hg38UCSC Ensembl
chr2:17797768..17797978hg19UCSC Ensembl
Cytoband2p24.2
Allele length
AssemblyAllele length
hg38211
hg19211
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5447510
Supporting Variants
Samples
Known GenesVSNL1
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16909238
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.000156


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