A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5687571



Internal ID21713892
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:14990133..14990133hg38UCSC Ensembl
chr6:14990364..14990364hg19UCSC Ensembl
Cytoband6p23
Allele length
AssemblyAllele length
hg38206
hg19206
Variant TypeCNV alu insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17224804
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)nsv5687571
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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