A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17190382



Internal ID21637891
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:15536814..15536814hg38UCSC Ensembl
chr11:15558360..15558360hg19UCSC Ensembl
Cytoband11p15.2
Allele length
AssemblyAllele length
hg38250
hg19250
Variant TypeCNV alu insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5697840
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)nssv17190382
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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