A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5482031



Internal ID259494
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:33733574..33734298hg38UCSC Ensembl
chr8:33591092..33591816hg19UCSC Ensembl
Cytoband8p12
Allele length
AssemblyAllele length
hg38725
hg19725
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17011310
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5482031
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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