A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5480328



Internal ID257836
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:76398626..76398690hg38UCSC Ensembl
chr9:79013542..79013606hg19UCSC Ensembl
Cytoband9q21.13
Allele length
AssemblyAllele length
hg3865
hg1965
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17022708
Samples
Known GenesRPSAP9
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5480328
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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