A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3417702



Internal ID19501991
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:62261501..62370100hg38UCSC Ensembl
chr9:46572802..46681401hg19UCSC Ensembl
Cytoband9p11.2
Allele length
AssemblyAllele length
hg38108600
hg19108600
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14777775, nssv14785143, nssv14773008, nssv14789401, nssv14783072, nssv14772238, nssv14775133, nssv14788056, nssv14772398, nssv14772430, nssv14782670, nssv14772471, nssv14773384, nssv14774252
SamplesCHM13, HG02106, HG04217, CHM1, 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)nsv3417702
Frequency
Sample Size14
Observed Gain14
Observed Loss0
Observed Complex0
Frequencyn/a


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