A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3560305



Internal ID22429102
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:85787429..85787429hg38UCSC Ensembl
chr13:86361564..86361564hg19UCSC Ensembl
Cytoband13q31.1
Allele length
AssemblyAllele length
hg38111
hg19111
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14369921, nssv14369922, nssv14369923
SamplesHG00512, HG00732, HG00513
Known Genes
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3560305
Frequency
Sample Size9
Observed Gain3
Observed Loss0
Observed Complex0
Frequencyn/a


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