A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3406653



Internal ID19837630
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:38101..48400hg38UCSC Ensembl
chr9:38101..48400hg19UCSC Ensembl
Cytoband9p24.3
Allele length
AssemblyAllele length
hg3810300
hg1910300
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14774667, nssv14781471, nssv14786313, nssv14777388, nssv14788832, nssv14786005, nssv14773903, nssv14785914, nssv14790343, nssv14774849, nssv14779433, nssv14780841, nssv14777935
SamplesCHM13, HG02106, HG04217, HG00268, NA12878, HG02818, HX1, HG02059, HG01352, NA19434, NA19240, HG00733, HG00514
Known Genes
MethodSequencing
AnalysisRead and contig alignments were done with BLASR. The Celera assembler (8.3rc2) was used to assemble RS II samples (CHM1, CHM13, HG00514, HG00733, NA19240, HG02818, NA19434, HG01352, HG02059, NA12878, and HG04217, and Canu (1.7) was used for Sequel samples (HG02106 and HG00268). Variant calling was performed with SMRT-SV (10.1101/gr.214007.116).
PlatformPacBio RS II P6C4, PacBio Sequel v2.1
Comments
ReferenceAudano_et_al_2019
Pubmed ID30661756
Accession Number(s)nsv3406653
Frequency
Sample Size14
Observed Gain13
Observed Loss0
Observed Complex0
Frequencyn/a


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