A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3565859



Internal ID22434568
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:112138242..112138242hg38UCSC Ensembl
chr9:114900522..114900522hg19UCSC Ensembl
Cytoband9q32
Allele length
AssemblyAllele length
hg3874
hg1974
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14349051, nssv14349052
SamplesHG00731, HG00733
Known GenesMIR3134, SUSD1
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3565859
Frequency
Sample Size9
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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