A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5699097



Internal ID21725418
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:15837740..15837740hg38UCSC Ensembl
chr10:15879739..15879739hg19UCSC Ensembl
Cytoband10p13
Allele length
AssemblyAllele length
hg38280
hg19280
Variant TypeCNV alu insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17187691
Samples
Known GenesFAM188A
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)nsv5699097
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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