A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3339864



Internal ID19424156
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:57403118..57403173hg38UCSC Ensembl
chr16:57437030..57437085hg19UCSC Ensembl
Cytoband16q21
Allele length
AssemblyAllele length
hg3856
hg1956
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14587527, nssv14577458, nssv14584840, nssv14583662, nssv14574026, nssv14580806
SamplesHG02106, NA12878, HG02059, HG01352, NA19434, 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)nsv3339864
Frequency
Sample Size14
Observed Gain0
Observed Loss6
Observed Complex0
Frequencyn/a


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