A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16921455



Internal ID15070
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:164330253..164330378hg38UCSC Ensembl
chr2:165186763..165186888hg19UCSC Ensembl
Cytoband2q24.3
Allele length
AssemblyAllele length
hg38126
hg19126
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5444737
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16921455
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.000156


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