A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5463692



Internal ID241587
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:132075710..132115141hg38UCSC Ensembl
chr6:132396850..132436281hg19UCSC Ensembl
Cytoband6q23.2
Allele length
AssemblyAllele length
hg3839432
hg1939432
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16970035
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5463692
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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