A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17246411



Internal ID21693920
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:26384136..26384136hg38UCSC Ensembl
chr10:26673065..26673065hg19UCSC Ensembl
Cytoband10p12.1
Allele length
AssemblyAllele length
hg383798
hg193798
Variant TypeCNV line1 insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5717990
Supporting Variants
Samples
Known Genes
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)nssv17246411
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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