A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5437424



Internal ID216014
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:23859461..23859591hg38UCSC Ensembl
chr2:24082331..24082461hg19UCSC Ensembl
Cytoband2p23.3
Allele length
AssemblyAllele length
hg38131
hg19131
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16910258
Samples
Known GenesATAD2B
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5437424
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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