A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5407029



Internal ID186365
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:87662004..87662055hg38UCSC Ensembl
chr10:89421761..89421812hg19UCSC Ensembl
Cytoband10q23.2
Allele length
AssemblyAllele length
hg38232
hg19232
Variant TypeCNV alu insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17038382
Samples
Known GenesPAPSS2
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5407029
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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