A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3327800



Internal ID19758778
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:133770001..133786900hg38UCSC Ensembl
chr10:135507326..135524225hg19UCSC Ensembl
Cytoband10q26.3
Allele length
AssemblyAllele length
hg3816900
hg1916900
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14497138, nssv14504646, nssv14508559, nssv14504099, nssv14510528, nssv14499741, nssv14497303, nssv14508187, nssv14498535, nssv14511051, nssv14493550
SamplesCHM13, HG04217, CHM1, NA12878, HG02818, HG02059, HG01352, NA19434, NA19240, HG00733, HG00514
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)nsv3327800
Frequency
Sample Size14
Observed Gain11
Observed Loss0
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer