A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5918254



Internal ID22693475
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:132526542..132529522hg38UCSC Ensembl
chr9:135401929..135404909hg19UCSC Ensembl
Cytoband9q34.13
Allele length
AssemblyAllele length
hg382981
hg192981
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17448124
Samples
Known GenesC9orf171
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5918254
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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