A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5489633



Internal ID266907
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:38378684..38378772hg38UCSC Ensembl
chr9:38378681..38378769hg19UCSC Ensembl
Cytoband9p13.2
Allele length
AssemblyAllele length
hg3889
hg1989
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17022885
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5489633
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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