A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4731384



Internal ID20507304
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:184366401..184366584hg38UCSC Ensembl
chr3:184084189..184084372hg19UCSC Ensembl
Cytoband3q27.1
Allele length
AssemblyAllele length
hg38184
hg19184
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16276271
Samples
Known GenesPOLR2H
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nsv4731384
Frequency
Sample Size25
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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