A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5477213



Internal ID254801
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:32714000..32733500hg38UCSC Ensembl
chr9:32713998..32733498hg19UCSC Ensembl
Cytoband9p21.1
Allele length
AssemblyAllele length
hg3819501
hg1919501
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17023465
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5477213
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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