A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17237585



Internal ID21685094
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:173338481..173338481hg38UCSC Ensembl
chr1:173307620..173307620hg19UCSC Ensembl
Cytoband1q25.1
Allele length
AssemblyAllele length
hg383267
hg193267
Variant TypeCNV line1 insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5728240
Supporting Variants
Samples
Known GenesLOC100506023
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)nssv17237585
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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