A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16910274



Internal ID7621
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:24035938..24036352hg38UCSC Ensembl
chr2:24258808..24259222hg19UCSC Ensembl
Cytoband2p23.3
Allele length
AssemblyAllele length
hg38415
hg19415
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5450923
Supporting Variants
Samples
Known GenesC2orf44
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16910274
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.000156


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