A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5709722



Internal ID21736043
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:46851283..46851283hg38UCSC Ensembl
chr13:47425418..47425418hg19UCSC Ensembl
Cytoband13q14.2
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 Variantsnssv17193924
Samples
Known GenesHTR2A
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)nsv5709722
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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