A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5486208



Internal ID263579
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:112208479..112210460hg38UCSC Ensembl
chr9:114970759..114972740hg19UCSC Ensembl
Cytoband9q32
Allele length
AssemblyAllele length
hg381982
hg191982
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17026299
Samples
Known GenesMIR3134
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5486208
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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