A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5710624



Internal ID21736945
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr18:22445010..22445010hg38UCSC Ensembl
chr18:20024973..20024973hg19UCSC Ensembl
Cytoband18q11.2
Allele length
AssemblyAllele length
hg38273
hg19273
Variant TypeCNV alu insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17198586, nssv17222405
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)nsv5710624
Frequency
Sample Size3202
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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