A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5700036



Internal ID21726357
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr18:13677803..13677803hg38UCSC Ensembl
chr18:13677802..13677802hg19UCSC Ensembl
Cytoband18p11.21
Allele length
AssemblyAllele length
hg38243
hg19243
Variant TypeCNV alu insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17200514
Samples
Known GenesFAM210A
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)nsv5700036
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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