A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5479231



Internal ID256761
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:87713190..87713263hg38UCSC Ensembl
chr9:90328105..90328178hg19UCSC Ensembl
Cytoband9q21.33
Allele length
AssemblyAllele length
hg3874
hg1974
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17025614
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5479231
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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