A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3565506



Internal ID22434225
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:101551616..101551616hg38UCSC Ensembl
chr9:104313898..104313898hg19UCSC Ensembl
Cytoband9q31.1
Allele length
AssemblyAllele length
hg3861
hg1961
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14349765, nssv14349762, nssv14349764, nssv14349763, nssv14349766
SamplesNA19238, NA19239, NA19240, HG00513, HG00514
Known GenesRNF20
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3565506
Frequency
Sample Size9
Observed Gain5
Observed Loss0
Observed Complex0
Frequencyn/a


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