A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5490319



Internal ID267576
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:133393667..133397296hg38UCSC Ensembl
chr9:136258794..136262423hg19UCSC Ensembl
Cytoband9q34.2
Allele length
AssemblyAllele length
hg383630
hg193630
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17030091
Samples
Known GenesC9orf96
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5490319
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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