A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3560260



Internal ID22429056
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:113279047..113279047hg38UCSC Ensembl
chr13:113933362..113933362hg19UCSC Ensembl
Cytoband13q34
Allele length
AssemblyAllele length
hg3883
hg1983
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14372194, nssv14372193
SamplesNA19238, NA19240
Known Genes
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3560260
Frequency
Sample Size9
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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