A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5409331



Internal ID188652
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:61269078..61269129hg38UCSC Ensembl
chr3:61254752..61254803hg19UCSC Ensembl
Cytoband3p14.2
Allele length
AssemblyAllele length
hg38281
hg19281
Variant TypeCNV alu insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16934693
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5409331
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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