A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5491086



Internal ID268331
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:112320252..112321479hg38UCSC Ensembl
chr9:115082532..115083759hg19UCSC Ensembl
Cytoband9q32
Allele length
AssemblyAllele length
hg381228
hg191228
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17026313
Samples
Known GenesMIR3134, PTBP3
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5491086
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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