A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5405902



Internal ID185243
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:2605730..2605781hg38UCSC Ensembl
chr5:2605844..2605895hg19UCSC Ensembl
Cytoband5p15.33
Allele length
AssemblyAllele length
hg3894
hg1994
Variant TypeCNV alu insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16963494
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5405902
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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