A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17590500



Internal ID21782543
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:133105834..133105834hg38UCSC Ensembl
chr9:135981221..135981221hg19UCSC Ensembl
Cytoband9q34.2
Allele length
AssemblyAllele length
hg3871
hg1971
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6095430
Supporting Variants
Samples
Known GenesRALGDS
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17590500
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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