A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16291584



Internal ID20500802
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:132526542..132529525hg38UCSC Ensembl
chr9:135401929..135404912hg19UCSC Ensembl
Cytoband9q34.13
Allele length
AssemblyAllele length
hg382984
hg192984
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4747923
Supporting Variants
Samples
Known GenesC9orf171
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nssv16291584
Frequency
Sample Size25
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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