A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17215606



Internal ID21663115
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:57848866..57848866hg38UCSC Ensembl
chr17:55926227..55926227hg19UCSC Ensembl
Cytoband17q22
Allele length
AssemblyAllele length
hg38280
hg19280
Variant TypeCNV alu insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5704659
Supporting Variants
Samples
Known GenesMRPS23
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)nssv17215606
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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