A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3560472



Internal ID22429269
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:71768286..71768286hg38UCSC Ensembl
chr15:72060625..72060625hg19UCSC Ensembl
Cytoband15q23
Allele length
AssemblyAllele length
hg38885
hg19885
Variant TypeCNV sva insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14389007
SamplesHG00731
Known GenesTHSD4
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)nsv3560472
Frequency
Sample Size9
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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