A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3560365



Internal ID22429162
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:77578810..77578810hg38UCSC Ensembl
chr14:78045153..78045153hg19UCSC Ensembl
Cytoband14q24.3
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 Variantsnssv14390526, nssv14388607
SamplesNA19239, HG00732
Known GenesSPTLC2
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)nsv3560365
Frequency
Sample Size9
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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