A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5475134



Internal ID252781
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:23404000..23450000hg38UCSC Ensembl
chr9:23403998..23449998hg19UCSC Ensembl
Cytoband9p21.3
Allele length
AssemblyAllele length
hg3846001
hg1946001
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17021939
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5475134
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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