A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4737833



Internal ID20513797
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:63270853..63270957hg38UCSC Ensembl
chr3:63256529..63256633hg19UCSC Ensembl
Cytoband3p14.2
Allele length
AssemblyAllele length
hg38105
hg19105
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16266335
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nsv4737833
Frequency
Sample Size25
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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