A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5395729



Internal ID175151
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:31169092..31169092hg38UCSC Ensembl
chr3:31210584..31210584hg19UCSC Ensembl
Cytoband3p23
Allele length
AssemblyAllele length
hg38312
hg19312
Variant TypeCNV alu insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16930465
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5395729
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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