A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5485467



Internal ID262856
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:95777084..95777140hg38UCSC Ensembl
chr9:98539366..98539422hg19UCSC Ensembl
Cytoband9q22.32
Allele length
AssemblyAllele length
hg3857
hg1957
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17027496
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5485467
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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