A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5729840



Internal ID21756161
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrY:11384829..11384829hg38UCSC Ensembl
chrY:13540505..13540505hg19UCSC Ensembl
CytobandYq11.21
Allele length
AssemblyAllele length
hg38164
hg19164
Variant TypeCNV alu insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17203571
Samples
Known Genes
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)nsv5729840
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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