A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5435083



Internal ID213737
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:152589134..152589370hg38UCSC Ensembl
chr3:152306923..152307159hg19UCSC Ensembl
Cytoband3q25.2
Allele length
AssemblyAllele length
hg38237
hg19237
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16939055
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5435083
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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