A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5477648



Internal ID255222
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:72380033..72380147hg38UCSC Ensembl
chr9:74994949..74995063hg19UCSC Ensembl
Cytoband9q21.13
Allele length
AssemblyAllele length
hg38115
hg19115
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17024317
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5477648
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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