A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5997274



Internal ID21906617
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:42287901..42287978hg38UCSC Ensembl
chr4:42289918..42289995hg19UCSC Ensembl
Cytoband4p13
Allele length
AssemblyAllele length
hg3878
hg1978
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17537948
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv5997274
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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