A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5480528



Internal ID258035
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:28533625..28735709hg38UCSC Ensembl
chr9:28533623..28735707hg19UCSC Ensembl
Cytoband9p21.1
Allele length
AssemblyAllele length
hg38202085
hg19202085
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv539n206
Supporting Variantsnssv17022061
Samples
Known GenesLINGO2
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5480528
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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