A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5679873



Internal ID21706194
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:85577597..85577597hg38UCSC Ensembl
chr1:86043280..86043280hg19UCSC Ensembl
Cytoband1p22.3
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 Variantsnssv17206160, nssv17173738
Samples
Known GenesDDAH1
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)nsv5679873
Frequency
Sample Size3202
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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