A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5462894



Internal ID240815
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:49481315..49482748hg38UCSC Ensembl
chr6:49449028..49450461hg19UCSC Ensembl
Cytoband6p12.3
Allele length
AssemblyAllele length
hg381434
hg191434
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16983247
Samples
Known GenesCENPQ
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5462894
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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