A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3377187



Internal ID19808165
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:179901188..179901239hg38UCSC Ensembl
chr3:179618976..179619027hg19UCSC Ensembl
Cytoband3q26.33
Allele length
AssemblyAllele length
hg3852
hg1952
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14676880, nssv14689380, nssv14675625, nssv14677206, nssv14684195, nssv14686929, nssv14678377, nssv14691686, nssv14675414, nssv14675490, nssv14672509, nssv14687028
SamplesCHM13, HG04217, CHM1, HG00268, NA12878, HG02818, HG02059, HG01352, NA19434, NA19240, HG00733, HG00514
Known GenesPEX5L
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)nsv3377187
Frequency
Sample Size14
Observed Gain0
Observed Loss12
Observed Complex0
Frequencyn/a


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