A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3560010



Internal ID22428805
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:109694117..109694117hg38UCSC Ensembl
chr13:110346464..110346464hg19UCSC Ensembl
Cytoband13q34
Allele length
AssemblyAllele length
hg3886
hg1986
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14368644, nssv14368645
SamplesNA19238, NA19240
Known Genes
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3560010
Frequency
Sample Size9
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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