A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5708056



Internal ID21734377
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:98137992..98137992hg38UCSC Ensembl
chr10:99897749..99897749hg19UCSC Ensembl
Cytoband10q24.2
Allele length
AssemblyAllele length
hg38279
hg19279
Variant TypeCNV alu insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17188339, nssv17214160
Samples
Known GenesR3HCC1L
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)nsv5708056
Frequency
Sample Size3202
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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