A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5447935



Internal ID226224
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:111129000..111129139hg38UCSC Ensembl
chr2:111886577..111886716hg19UCSC Ensembl
Cytoband2q13
Allele length
AssemblyAllele length
hg38140
hg19140
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16918758
Samples
Known GenesBCL2L11
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5447935
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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