A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3565529



Internal ID22434247
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:35018979..35018979hg38UCSC Ensembl
chr9:35018976..35018976hg19UCSC Ensembl
Cytoband9p13.3
Allele length
AssemblyAllele length
hg3864
hg1964
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14346398, nssv14346397, nssv14346399, nssv14346400
SamplesNA19238, HG00731, HG00732, HG00733
Known Genes
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3565529
Frequency
Sample Size9
Observed Gain4
Observed Loss0
Observed Complex0
Frequencyn/a


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