A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5476142



Internal ID253760
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:82685559..82686108hg38UCSC Ensembl
chr9:85300474..85301023hg19UCSC Ensembl
Cytoband9q21.32
Allele length
AssemblyAllele length
hg38550
hg19550
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17025333
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5476142
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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