A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4732408



Internal ID20508332
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:153301225..153301347hg38UCSC Ensembl
chr3:153019014..153019136hg19UCSC Ensembl
Cytoband3q25.2
Allele length
AssemblyAllele length
hg38123
hg19123
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16296017
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nsv4732408
Frequency
Sample Size25
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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