A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16920173



Internal ID14230
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:156048718..156051323hg38UCSC Ensembl
chr2:156905230..156907835hg19UCSC Ensembl
Cytoband2q24.1
Allele length
AssemblyAllele length
hg382606
hg192606
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5435360
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16920173
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.000312


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