A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3320331



Internal ID19751309
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:144768501..144813400hg38UCSC Ensembl
chr2:91750834..91795593hg19UCSC Ensembl
Cytoband2p11.1
Allele length
AssemblyAllele length
hg3844900
hg1944760
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14482953, nssv14484507, nssv14486824, nssv14474535, nssv14488391, nssv14483847, nssv14489889, nssv14484442, nssv14476294, nssv14476728, nssv14484920, nssv14478317
SamplesCHM13, HG02106, HG04217, CHM1, HG00268, NA12878, HG02818, HG02059, HG01352, NA19434, NA19240, 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)nsv3320331
Frequency
Sample Size14
Observed Gain12
Observed Loss0
Observed Complex0
Frequencyn/a


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