A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17214155



Internal ID21661664
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:15245517..15245517hg38UCSC Ensembl
chrX:15263639..15263639hg19UCSC Ensembl
CytobandXp22.2
Allele length
AssemblyAllele length
hg38947
hg19947
Variant TypeCNV line1 insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5730707
Supporting Variants
Samples
Known GenesASB9
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)nssv17214155
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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