A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17251949



Internal ID21699458
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:85138358..85138358hg38UCSC Ensembl
chr6:85848076..85848076hg19UCSC Ensembl
Cytoband6q14.3
Allele length
AssemblyAllele length
hg386014
hg196014
Variant TypeCNV line1 insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5718771
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)nssv17251949
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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