A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5458912



Internal ID236932
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:69175270..69175322hg38UCSC Ensembl
chr5:68471097..68471149hg19UCSC Ensembl
Cytoband5q13.2
Allele length
AssemblyAllele length
hg3853
hg1953
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16967388
Samples
Known GenesCCNB1
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5458912
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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