A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3353837



Internal ID19784815
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr18:65866004..65866347hg38UCSC Ensembl
chr18:63533240..63533583hg19UCSC Ensembl
Cytoband18q22.1
Allele length
AssemblyAllele length
hg38344
hg19344
Variant TypeCNV alu deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14555314, nssv14557825, nssv14566215, nssv14566565, nssv14567525, nssv14557162, nssv14554578, nssv14558645, nssv14552872, nssv14557723, nssv14571612, nssv14570797
SamplesCHM13, HG02106, HG04217, CHM1, HG00268, NA12878, HG02818, HX1, HG01352, NA19434, NA19240, HG00514
Known GenesCDH7
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 Alu insertion that is present in the reference
ReferenceAudano_et_al_2019
Pubmed ID30661756
Accession Number(s)nsv3353837
Frequency
Sample Size14
Observed Gain0
Observed Loss12
Observed Complex0
Frequencyn/a


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