A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17028085



Internal ID86420
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:129425552..129444552hg38UCSC Ensembl
chr9:132187831..132206831hg19UCSC Ensembl
Cytoband9q34.11
Allele length
AssemblyAllele length
hg3819001
hg1919001
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6142828
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17028085
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.682383


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