A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5402406



Internal ID181776
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:121635936..121635987hg38UCSC Ensembl
chr10:123395450..123395501hg19UCSC Ensembl
Cytoband10q26.13
Allele length
AssemblyAllele length
hg38280
hg19280
Variant TypeCNV alu insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17037863
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5402406
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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