A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16910540



Internal ID7798
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:24405430..24406182hg38UCSC Ensembl
chr2:24628299..24629051hg19UCSC Ensembl
Cytoband2p23.3
Allele length
AssemblyAllele length
hg38753
hg19753
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5446495
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16910540
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.000468


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