A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5406244



Internal ID185585
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:6159190..6159233hg38UCSC Ensembl
chr5:6159303..6159346hg19UCSC Ensembl
Cytoband5p15.32
Allele length
AssemblyAllele length
hg38313
hg19313
Variant TypeCNV alu insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16961898
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5406244
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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