A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16910949



Internal ID8064
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:22962000..22985000hg38UCSC Ensembl
chr2:23184872..23207872hg19UCSC Ensembl
Cytoband2p24.1
Allele length
AssemblyAllele length
hg3823001
hg1923001
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5438495
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16910949
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.000156


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