A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17025885



Internal ID84994
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:65538000..65584623hg38UCSC Ensembl
chr9:44814728..44861456hg19UCSC Ensembl
Cytoband9p11.2
Allele length
AssemblyAllele length
hg3846624
hg1946729
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5479355
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17025885
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.004075


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