A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5484801



Internal ID262207
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:5516631..5516781hg38UCSC Ensembl
chr9:5516631..5516781hg19UCSC Ensembl
Cytoband9p24.1
Allele length
AssemblyAllele length
hg38151
hg19151
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17020997
Samples
Known GenesPDCD1LG2
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5484801
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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