A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17431037



Internal ID22488907
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:94917131..94917184hg38UCSC Ensembl
chr9:97679413..97679466hg19UCSC Ensembl
Cytoband9q22.32
Allele length
AssemblyAllele length
hg3854
hg1954
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5915947
Supporting Variants
Samples
Known GenesC9orf3
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17431037
Frequency
Sample Size914
Observed Gain1
Observed Loss0
Observed Complex0
Frequency1.00


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