A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5492835



Internal ID270034
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:1194277..1486662hg38UCSC Ensembl
chr9:1194277..1486662hg19UCSC Ensembl
Cytoband9p24.3
Allele length
AssemblyAllele length
hg38292386
hg19292386
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv520n206
Supporting Variantsnssv17017782
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5492835
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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