A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3216338



Internal ID22362361
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:85822809..85882394hg38UCSC Ensembl
chr10:87582566..87642151hg19UCSC Ensembl
Cytoband10q23.1
Allele length
AssemblyAllele length
hg3859586
hg1959586
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14354847, nssv14354846
SamplesHG00513, HG00514
Known GenesGRID1
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3216338
Frequency
Sample Size9
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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