A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5453695



Internal ID231809
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:150608907..150609024hg38UCSC Ensembl
chr3:150326694..150326811hg19UCSC Ensembl
Cytoband3q25.1
Allele length
AssemblyAllele length
hg38118
hg19118
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16940539
Samples
Known GenesSELT
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5453695
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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