A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5994402



Internal ID21903745
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:61430347..61431131hg38UCSC Ensembl
chr3:61416021..61416805hg19UCSC Ensembl
Cytoband3p14.2
Allele length
AssemblyAllele length
hg38785
hg19785
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17550068
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv5994402
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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