A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3559765



Internal ID22428561
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:12832893..12832893hg38UCSC Ensembl
chr11:12854440..12854440hg19UCSC Ensembl
Cytoband11p15.2
Allele length
AssemblyAllele length
hg381267
hg191267
Variant TypeCNV sva insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14355304
SamplesHG00731
Known GenesTEAD1
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
CommentsInsertion of a SVA mobile element relative to the reference
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3559765
Frequency
Sample Size9
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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