A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3402190



Internal ID19833166
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:320860..321042hg38UCSC Ensembl
chr9:320860..321042hg19UCSC Ensembl
Cytoband9p24.3
Allele length
AssemblyAllele length
hg38183
hg19183
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14779885, nssv14789700, nssv14781498
SamplesNA12878, HG02818, NA19240
Known GenesDOCK8
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)nsv3402190
Frequency
Sample Size14
Observed Gain0
Observed Loss3
Observed Complex0
Frequencyn/a


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