A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5996266



Internal ID21905609
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:183768159..183768568hg38UCSC Ensembl
chr4:184689312..184689721hg19UCSC Ensembl
Cytoband4q35.1
Allele length
AssemblyAllele length
hg38410
hg19410
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17548716
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv5996266
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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