A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3322370



Internal ID19753348
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:234669967..234669967hg38UCSC Ensembl
chr1:234805713..234805713hg19UCSC Ensembl
Cytoband1q42.3
Allele length
AssemblyAllele length
hg38331
hg19331
Variant TypeCNV alu insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14506007, nssv14510849, nssv14492212, nssv14495146, nssv14506611, nssv14498227, nssv14500442, nssv14503659
SamplesCHM13, HG02106, HG04217, NA12878, HG02818, 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)nsv3322370
Frequency
Sample Size14
Observed Gain8
Observed Loss0
Observed Complex0
Frequencyn/a


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