A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17584852



Internal ID21776895
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 Variantsnsv6014646
Supporting Variants
Samples
Known GenesC9orf171
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17584852
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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