A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17230227



Internal ID21677736
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:69461865..69461865hg38UCSC Ensembl
chr15:69754204..69754204hg19UCSC Ensembl
Cytoband15q23
Allele length
AssemblyAllele length
hg3865
hg1965
Variant TypeCNV alu insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5714161
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)nssv17230227
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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