A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16913558



Internal ID9782
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:58315716..58315716hg38UCSC Ensembl
chr2:58542851..58542851hg19UCSC Ensembl
Cytoband2p16.1
Allele length
AssemblyAllele length
hg38436
hg19436
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5545374
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16913558
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.004484


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