A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17025764



Internal ID84913
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:94362648..94368488hg38UCSC Ensembl
chr9:97124930..97130770hg19UCSC Ensembl
Cytoband9q22.32
Allele length
AssemblyAllele length
hg385841
hg195841
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5476228
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17025764
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.000156


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