A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5677735



Internal ID21704056
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:112096701..112096701hg38UCSC Ensembl
chr6:112417904..112417904hg19UCSC Ensembl
Cytoband6q21
Allele length
AssemblyAllele length
hg38261
hg19261
Variant TypeCNV alu insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17179609, nssv17217122
Samples
Known GenesFAM229B
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)nsv5677735
Frequency
Sample Size3202
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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