A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5703036



Internal ID21729357
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:109892797..109892797hg38UCSC Ensembl
chr10:111652555..111652555hg19UCSC Ensembl
Cytoband10q25.1
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 Variantsnssv17189749, nssv17231996
Samples
Known GenesXPNPEP1
MethodSequencing
AnalysisMobile Element Locator Tool (MELT)
Platform
CommentsInsertion of a Alu mobile element relative to the reference
ReferenceChuang_et_al_2021
Pubmed ID34772701
Accession Number(s)nsv5703036
Frequency
Sample Size3202
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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