A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5905030



Internal ID22680211
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:146224873..146225082hg38UCSC Ensembl
chr3:145942660..145942869hg19UCSC Ensembl
Cytoband3q24
Allele length
AssemblyAllele length
hg38210
hg19210
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17428408
Samples
Known GenesPLSCR4
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5905030
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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