A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17223519



Internal ID21671028
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:69021582..69021582hg38UCSC Ensembl
chr1:69487265..69487265hg19UCSC Ensembl
Cytoband1p31.2
Allele length
AssemblyAllele length
hg38280
hg19280
Variant TypeCNV alu insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5694129
Supporting Variants
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)nssv17223519
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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