A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17249596



Internal ID21697105
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:121085594..121085594hg38UCSC Ensembl
chr6:121406740..121406740hg19UCSC Ensembl
Cytoband6q22.31
Allele length
AssemblyAllele length
hg386015
hg196015
Variant TypeCNV line1 insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5720347
Supporting Variants
Samples
Known GenesTBC1D32
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)nssv17249596
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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