A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5995979



Internal ID21905322
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:16909862..16935298hg38UCSC Ensembl
chr4:16911485..16936921hg19UCSC Ensembl
Cytoband4p15.32
Allele length
AssemblyAllele length
hg3825437
hg1925437
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17542512
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv5995979
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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