A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3396852



Internal ID19481143
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:90493107..90493107hg38UCSC Ensembl
chr5:89788924..89788924hg19UCSC Ensembl
Cytoband5q14.3
Allele length
AssemblyAllele length
hg38288
hg19288
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14721571, nssv14719497, nssv14718015
SamplesHG04217, HX1, NA19434
Known GenesPOLR3G
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)nsv3396852
Frequency
Sample Size14
Observed Gain3
Observed Loss0
Observed Complex0
Frequencyn/a


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