A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5480460



Internal ID257969
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:79082000..79093000hg38UCSC Ensembl
chr9:81696916..81707916hg19UCSC Ensembl
Cytoband9q21.31
Allele length
AssemblyAllele length
hg3811001
hg1911001
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17024484
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5480460
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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