A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5483497



Internal ID260933
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:96183129..96183317hg38UCSC Ensembl
chr9:98945411..98945599hg19UCSC Ensembl
Cytoband9q22.32
Allele length
AssemblyAllele length
hg38189
hg19189
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17025848
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5483497
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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