A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17586761



Internal ID21778804
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:104060651..104060651hg38UCSC Ensembl
chr9:106822932..106822932hg19UCSC Ensembl
Cytoband9q31.1
Allele length
AssemblyAllele length
hg38311
hg19311
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6085498
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17586761
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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