A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16912026



Internal ID8770
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:32122517..32125412hg38UCSC Ensembl
chr2:32347586..32350481hg19UCSC Ensembl
Cytoband2p22.3
Allele length
AssemblyAllele length
hg382896
hg192896
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5439253
Supporting Variants
Samples
Known GenesSPAST
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16912026
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.000156


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