A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5527743



Internal ID303827
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:59109990..59112962hg38UCSC Ensembl
chr15:59402189..59405161hg19UCSC Ensembl
Cytoband15q22.2
Allele length
AssemblyAllele length
hg382973
hg192973
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17700945
Samples
Known GenesCCNB2
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5527743
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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