A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17025888



Internal ID84997
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 StatusS
Merged Variantsnsv5490693
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17025888
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.004222


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