A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17201570



Internal ID21649079
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr18:55333525..55333525hg38UCSC Ensembl
chr18:53000756..53000756hg19UCSC Ensembl
Cytoband18q21.2
Allele length
AssemblyAllele length
hg38280
hg19280
Variant TypeCNV alu insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5708345
Supporting Variants
Samples
Known GenesTCF4
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)nssv17201570
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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