A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3222785



Internal ID22366755
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 Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14352880, nssv14352879, nssv14352878, nssv14352883, nssv14352876, nssv14352875, nssv14352882, nssv14352881, nssv14352877
SamplesHG00512, NA19238, NA19239, HG00731, HG00732, NA19240, HG00733, HG00513, HG00514
Known GenesHPSE2
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3222785
Frequency
Sample Size9
Observed Gain9
Observed Loss0
Observed Complex0
Frequencyn/a


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