A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5485787



Internal ID263169
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:122773805..122773866hg38UCSC Ensembl
chr9:125536084..125536145hg19UCSC Ensembl
Cytoband9q33.2
Allele length
AssemblyAllele length
hg3862
hg1962
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17027123
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5485787
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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