A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3411331



Internal ID19842307
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:143015717..143015803hg38UCSC Ensembl
chr8:144097134..144097220hg19UCSC Ensembl
Cytoband8q24.3
Allele length
AssemblyAllele length
hg3887
hg1987
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14773450, nssv14775379, nssv14784740, nssv14774635, nssv14780811
SamplesCHM13, HG02106, HG02059, NA19434, HG00733
Known GenesLOC100133669
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)nsv3411331
Frequency
Sample Size14
Observed Gain0
Observed Loss5
Observed Complex0
Frequencyn/a


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