A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5404400



Internal ID183753
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:31381863..31381914hg38UCSC Ensembl
chr3:31423355..31423406hg19UCSC Ensembl
Cytoband3p23
Allele length
AssemblyAllele length
hg38107
hg19107
Variant TypeCNV alu insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16932140
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5404400
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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