A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5434538



Internal ID213211
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:23876833..23878100hg38UCSC Ensembl
chr2:24099703..24100970hg19UCSC Ensembl
Cytoband2p23.3
Allele length
AssemblyAllele length
hg381268
hg191268
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16910259
Samples
Known GenesATAD2B
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5434538
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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