A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16920627



Internal ID14531
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:156218123..156223198hg38UCSC Ensembl
chr2:157074635..157079710hg19UCSC Ensembl
Cytoband2q24.1
Allele length
AssemblyAllele length
hg385076
hg195076
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5442288
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16920627
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.000312


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