A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17236527



Internal ID21684036
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:34287705..34287705hg38UCSC Ensembl
chr17:32614724..32614724hg19UCSC Ensembl
Cytoband17q12
Allele length
AssemblyAllele length
hg383281
hg193281
Variant TypeCNV line1 insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5728195
Supporting Variants
Samples
Known GenesCCL11
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)nssv17236527
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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