A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5399683



Internal ID179071
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:108690880..108690880hg38UCSC Ensembl
chr5:108026581..108026581hg19UCSC Ensembl
Cytoband5q21.3
Allele length
AssemblyAllele length
hg38311
hg19311
Variant TypeCNV alu insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16973598
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5399683
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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