A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5684664



Internal ID21710985
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:41362907..41362907hg38UCSC Ensembl
chr4:41364924..41364924hg19UCSC Ensembl
Cytoband4p13
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 Variantsnssv17208634, nssv17230425
Samples
Known GenesLIMCH1
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)nsv5684664
Frequency
Sample Size3202
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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