A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3415192



Internal ID19846169
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:101358930..101358930hg38UCSC Ensembl
chr9:104121212..104121212hg19UCSC Ensembl
Cytoband9q31.1
Allele length
AssemblyAllele length
hg389562
hg199562
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14788040, nssv14790435, nssv14782397, nssv14776908
SamplesHG00268, HG02818, NA19434, HG00733
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)nsv3415192
Frequency
Sample Size14
Observed Gain4
Observed Loss0
Observed Complex0
Frequencyn/a


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