A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3560024



Internal ID22428819
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:26122913..26122913hg38UCSC Ensembl
chr13:26697051..26697051hg19UCSC Ensembl
Cytoband13q12.13
Allele length
AssemblyAllele length
hg3858
hg1958
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14367432, nssv14367431
SamplesNA19239, NA19240
Known Genes
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3560024
Frequency
Sample Size9
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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