A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3559394



Internal ID22428197
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:99625152..99625152hg38UCSC Ensembl
chr10:101384909..101384909hg19UCSC Ensembl
Cytoband10q24.2
Allele length
AssemblyAllele length
hg38102
hg19102
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14352924, nssv14352920, nssv14352923, nssv14352919, nssv14352922, nssv14352921
SamplesHG00512, HG00731, HG00732, HG00733, HG00513, HG00514
Known Genes
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3559394
Frequency
Sample Size9
Observed Gain6
Observed Loss0
Observed Complex0
Frequencyn/a


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