A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5485555



Internal ID262944
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:1523582..1625441hg38UCSC Ensembl
chr9:1523582..1625441hg19UCSC Ensembl
Cytoband9p24.3
Allele length
AssemblyAllele length
hg38101860
hg19101860
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17017813
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5485555
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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