A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5995142



Internal ID21904485
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:128665288..128665373hg38UCSC Ensembl
chr4:129586443..129586528hg19UCSC Ensembl
Cytoband4q28.2
Allele length
AssemblyAllele length
hg3886
hg1986
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17543062
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv5995142
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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