A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5995199



Internal ID21904542
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:13914146..13914713hg38UCSC Ensembl
chr4:13915770..13916337hg19UCSC Ensembl
Cytoband4p15.33
Allele length
AssemblyAllele length
hg38568
hg19568
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17546279
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv5995199
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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