A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5713419



Internal ID21739740
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:76636388..76636388hg38UCSC Ensembl
chr10:78396146..78396146hg19UCSC Ensembl
Cytoband10q22.3
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 Variantsnssv17214651, nssv17189087
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)nsv5713419
Frequency
Sample Size3202
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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