A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5686675



Internal ID21712996
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:148513853..148513853hg38UCSC Ensembl
chr6:148834989..148834989hg19UCSC Ensembl
Cytoband6q24.3
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 Variantsnssv17217330, nssv17180698
Samples
Known GenesSASH1
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)nsv5686675
Frequency
Sample Size3202
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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