A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5485135



Internal ID262532
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:28014516..28014778hg38UCSC Ensembl
chr9:28014514..28014776hg19UCSC Ensembl
Cytoband9p21.1
Allele length
AssemblyAllele length
hg38263
hg19263
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17020254
Samples
Known GenesLINGO2
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5485135
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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