A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14352876



Internal ID22140272
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:98466927..98468503hg38UCSC Ensembl
chr10:100226684..100228260hg19UCSC Ensembl
Cytoband10q24.2
Allele length
AssemblyAllele length
hg381577
hg191577
Variant TypeCNV duplication
Copy Number2
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3222785
Supporting Variants
SamplesHG00513
Known GenesHPSE2
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nssv14352876
Frequency
Sample Size9
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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