A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5485377



Internal ID262767
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:6487570..6521838hg38UCSC Ensembl
chr9:6487570..6521838hg19UCSC Ensembl
Cytoband9p24.1
Allele length
AssemblyAllele length
hg3834269
hg1934269
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17019663
Samples
Known GenesUHRF2
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5485377
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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