A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3338994



Internal ID19769972
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:111429856..111429909hg38UCSC Ensembl
chr13:112082203..112082256hg19UCSC Ensembl
Cytoband13q34
Allele length
AssemblyAllele length
hg3854
hg1954
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14539920, nssv14538707, nssv14542947, nssv14539465, nssv14534865
SamplesHG00268, NA12878, HG02818, NA19434, 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)nsv3338994
Frequency
Sample Size14
Observed Gain0
Observed Loss5
Observed Complex0
Frequencyn/a


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