A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5403606



Internal ID182966
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:115818732..115818783hg38UCSC Ensembl
chr5:115154429..115154480hg19UCSC Ensembl
Cytoband5q22.3
Allele length
AssemblyAllele length
hg38280
hg19280
Variant TypeCNV alu insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16972981
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5403606
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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