A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3393578



Internal ID19477869
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:146971421..146971476hg38UCSC Ensembl
chr4:147892573..147892628hg19UCSC Ensembl
Cytoband4q31.22
Allele length
AssemblyAllele length
hg3856
hg1956
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14692992, nssv14695055, nssv14699384, nssv14710070, nssv14701662, nssv14702013, nssv14701529
SamplesNA12878, 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)nsv3393578
Frequency
Sample Size14
Observed Gain0
Observed Loss7
Observed Complex0
Frequencyn/a


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