A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3565426



Internal ID22434145
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:126074684..126074684hg38UCSC Ensembl
chr8:127086928..127086928hg19UCSC Ensembl
Cytoband8q24.13
Allele length
AssemblyAllele length
hg38113
hg19113
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14344979, nssv14344985, nssv14344984, nssv14344982, nssv14344980, nssv14344978, nssv14344986, nssv14344983, nssv14344981
SamplesHG00512, NA19238, NA19239, HG00731, HG00732, NA19240, HG00733, HG00513, HG00514
Known Genes
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3565426
Frequency
Sample Size9
Observed Gain9
Observed Loss0
Observed Complex0
Frequencyn/a


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