A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5479173



Internal ID256705
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:133386021..133386424hg38UCSC Ensembl
chr9:136251805..136252208hg19UCSC Ensembl
Cytoband9q34.2
Allele length
AssemblyAllele length
hg38404
hg19404
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17735916
Samples
Known GenesC9orf96
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5479173
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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