A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5488962



Internal ID266255
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:26641450..26694970hg38UCSC Ensembl
chr9:26641448..26694968hg19UCSC Ensembl
Cytoband9p21.2
Allele length
AssemblyAllele length
hg3853521
hg1953521
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17022856
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5488962
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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