A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16912355



Internal ID8987
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:33486101..33489876hg38UCSC Ensembl
chr2:33711168..33714943hg19UCSC Ensembl
Cytoband2p22.3
Allele length
AssemblyAllele length
hg383776
hg193776
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5437525
Supporting Variants
Samples
Known GenesRASGRP3
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16912355
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.000156


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