A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4745799



Internal ID20521809
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:132301750..132301976hg38UCSC Ensembl
chr3:132020594..132020820hg19UCSC Ensembl
Cytoband3q22.1
Allele length
AssemblyAllele length
hg38227
hg19227
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16279436
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nsv4745799
Frequency
Sample Size25
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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