A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5675726



Internal ID21702047
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:160915415..160915415hg38UCSC Ensembl
chr6:161336447..161336447hg19UCSC Ensembl
Cytoband6q26
Allele length
AssemblyAllele length
hg38279
hg19279
Variant TypeCNV alu insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17181241, nssv17222846
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)nsv5675726
Frequency
Sample Size3202
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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