A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5409539



Internal ID188860
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:71577713..71577764hg38UCSC Ensembl
chr5:70873540..70873591hg19UCSC Ensembl
Cytoband5q13.2
Allele length
AssemblyAllele length
hg38212
hg19212
Variant TypeCNV alu insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16966862
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5409539
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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