A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5403541



Internal ID182901
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:63596339..63596339hg38UCSC Ensembl
chr10:65356099..65356099hg19UCSC Ensembl
Cytoband10q21.3
Allele length
AssemblyAllele length
hg38324
hg19324
Variant TypeCNV alu insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17034073
Samples
Known GenesREEP3
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5403541
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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