A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5478485



Internal ID256038
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:25069635..25248414hg38UCSC Ensembl
chr9:25069633..25248412hg19UCSC Ensembl
Cytoband9p21.3
Allele length
AssemblyAllele length
hg38178780
hg19178780
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17022033
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5478485
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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