A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16922293



Internal ID15619
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:172412454..172412816hg38UCSC Ensembl
chr2:173277182..173277544hg19UCSC Ensembl
Cytoband2q31.1
Allele length
AssemblyAllele length
hg38363
hg19363
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5450355
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16922293
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.000312


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