A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5489780



Internal ID267051
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:36837764..36837860hg38UCSC Ensembl
chr9:36837761..36837857hg19UCSC Ensembl
Cytoband9p13.2
Allele length
AssemblyAllele length
hg3897
hg1997
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17024699
Samples
Known GenesPAX5
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5489780
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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