A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5490693



Internal ID267944
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:65567123..65573500hg38UCSC Ensembl
chr9:44843850..44850338hg19UCSC Ensembl
Cytoband9p11.2
Allele length
AssemblyAllele length
hg386378
hg196489
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17025888
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5490693
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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