A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5995771



Internal ID21905114
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:163093605..163097482hg38UCSC Ensembl
chr4:164014757..164018634hg19UCSC Ensembl
Cytoband4q32.2
Allele length
AssemblyAllele length
hg383878
hg193878
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17554229
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv5995771
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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