A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3356678



Internal ID19787656
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:43076801..43076801hg38UCSC Ensembl
chr15:43368999..43368999hg19UCSC Ensembl
Cytoband15q15.2
Allele length
AssemblyAllele length
hg38127
hg19127
Variant TypeCNV sva insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14568166, nssv14553069, nssv14563617, nssv14561961, nssv14559976, nssv14558316, nssv14566375, nssv14569168, nssv14562298, nssv14560400
SamplesCHM13, HG02106, HG04217, CHM1, HG00268, HG02818, HX1, HG02059, HG00733, HG00514
Known GenesUBR1
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)nsv3356678
Frequency
Sample Size14
Observed Gain10
Observed Loss0
Observed Complex0
Frequencyn/a


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