A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5487179



Internal ID264523
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:4735269..4735408hg38UCSC Ensembl
chr9:4735269..4735408hg19UCSC Ensembl
Cytoband9p24.1
Allele length
AssemblyAllele length
hg38140
hg19140
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17018848
Samples
Known GenesAK3
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5487179
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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