A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14797037



Internal ID19545009
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr18:5209666..5209898hg38UCSC Ensembl
chr18:5209665..5209897hg19UCSC Ensembl
Cytoband18p11.31
Allele length
AssemblyAllele length
hg38233
hg19233
Variant TypeCNV mobile element deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3344241
Supporting Variants
SamplesHG01352
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
CommentsAbsence of a mobile element insertion that is present in the reference
ReferenceAudano_et_al_2019
Pubmed ID30661756
Accession Number(s)nssv14797037
Frequency
Sample Size14
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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