A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5994456



Internal ID21903799
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:73833623..73833716hg38UCSC Ensembl
chr3:73882774..73882867hg19UCSC Ensembl
Cytoband3p13
Allele length
AssemblyAllele length
hg3894
hg1994
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17542143
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv5994456
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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