A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17581926



Internal ID21773969
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:93105931..93105931hg38UCSC Ensembl
chr9:95868213..95868213hg19UCSC Ensembl
Cytoband9q22.31
Allele length
AssemblyAllele length
hg38309
hg19309
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6088306
Supporting Variants
Samples
Known GenesC9orf89
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17581926
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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