A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5994513



Internal ID21903856
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:95014591..95074537hg38UCSC Ensembl
chr3:94733435..94793381hg19UCSC Ensembl
Cytoband3q11.2
Allele length
AssemblyAllele length
hg3859947
hg1959947
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17543602
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv5994513
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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