A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17203220



Internal ID21650729
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:36045869..36045869hg38UCSC Ensembl
chr20:34633791..34633791hg19UCSC Ensembl
Cytoband20q11.23
Allele length
AssemblyAllele length
hg38262
hg19262
Variant TypeCNV alu insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5713235
Supporting Variants
Samples
Known GenesLINC00657
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)nssv17203220
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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