A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17241411



Internal ID21688920
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:110195629..110195629hg38UCSC Ensembl
chrX:109438857..109438857hg19UCSC Ensembl
CytobandXq23
Allele length
AssemblyAllele length
hg38248
hg19248
Variant TypeCNV line1 insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5719111
Supporting Variants
Samples
Known GenesAMMECR1
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)nssv17241411
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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