A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5729860



Internal ID21756181
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:150626752..150626752hg38UCSC Ensembl
chrX:149795225..149795225hg19UCSC Ensembl
CytobandXq28
Allele length
AssemblyAllele length
hg38146
hg19146
Variant TypeCNV line1 insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17244103
Samples
Known GenesMTM1
MethodSequencing
AnalysisMobile Element Locator Tool (MELT)
Platform
CommentsInsertion of a L1 mobile element relative to the reference
ReferenceChuang_et_al_2021
Pubmed ID34772701
Accession Number(s)nsv5729860
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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