A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17193802



Internal ID21641311
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:20653605..20653605hg38UCSC Ensembl
chr13:21227744..21227744hg19UCSC Ensembl
Cytoband13q12.11
Allele length
AssemblyAllele length
hg38237
hg19237
Variant TypeCNV alu insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5705837
Supporting Variants
Samples
Known GenesIFT88
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)nssv17193802
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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