A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3326663



Internal ID19410955
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:101366890..101366890hg38UCSC Ensembl
chr10:103126647..103126647hg19UCSC Ensembl
Cytoband10q24.32
Allele length
AssemblyAllele length
hg3851
hg1951
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14495447, nssv14497974, nssv14509079
SamplesHG00268, HG02059, HG01352
Known GenesBTRC
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)nsv3326663
Frequency
Sample Size14
Observed Gain3
Observed Loss0
Observed Complex0
Frequencyn/a


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