A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3360169



Internal ID19791147
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:16309444..16309532hg38UCSC Ensembl
chr3:16350951..16351039hg19UCSC Ensembl
Cytoband3p25.1
Allele length
AssemblyAllele length
hg3889
hg1989
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14655960, nssv14661032, nssv14671394, nssv14666167, nssv14654094, nssv14666405, nssv14664654, nssv14660607, nssv14660061, nssv14668856, nssv14664382
SamplesHG02106, HG04217, CHM1, HG00268, NA12878, HG02818, HX1, HG02059, NA19434, NA19240, 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)nsv3360169
Frequency
Sample Size14
Observed Gain0
Observed Loss11
Observed Complex0
Frequencyn/a


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