A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3333532



Internal ID19764510
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:70126795..70126795hg38UCSC Ensembl
chr11:69972901..69972901hg19UCSC Ensembl
Cytoband11q13.3
Allele length
AssemblyAllele length
hg3898
hg1998
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14523418, nssv14513186, nssv14524639, nssv14512402, nssv14522048, nssv14528873
SamplesHG02106, CHM1, HG02059, NA19434, HG00733, HG00514
Known GenesANO1
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)nsv3333532
Frequency
Sample Size14
Observed Gain6
Observed Loss0
Observed Complex0
Frequencyn/a


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