A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5486698



Internal ID264056
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:35657732..35657802hg38UCSC Ensembl
chr9:35657729..35657799hg19UCSC Ensembl
Cytoband9p13.3
Allele length
AssemblyAllele length
hg3871
hg1971
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17023667
Samples
Known GenesRMRP
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5486698
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer