A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14539068



Internal ID19627059
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:19832901..19832901hg38UCSC Ensembl
chr13:20407041..20407041hg19UCSC Ensembl
Cytoband13q12.11
Allele length
AssemblyAllele length
hg38293
hg19293
Variant TypeCNV alu insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3358637
Supporting Variants
SamplesHG02818
Known GenesZMYM5
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)nssv14539068
Frequency
Sample Size14
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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