A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5483138



Internal ID260581
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:77017048..77017144hg38UCSC Ensembl
chr9:79631964..79632060hg19UCSC Ensembl
Cytoband9q21.2
Allele length
AssemblyAllele length
hg3897
hg1997
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17025915
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5483138
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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