A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5408693



Internal ID188017
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:122781916..122781967hg38UCSC Ensembl
chr10:124541432..124541483hg19UCSC 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 Variantsnssv17038829
Samples
Known GenesFLJ46361
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5408693
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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