A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3349098



Internal ID19780076
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:81669286..81669376hg38UCSC Ensembl
chr16:81702891..81702981hg19UCSC Ensembl
Cytoband16q23.3
Allele length
AssemblyAllele length
hg3891
hg1991
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14581322, nssv14572054, nssv14589229, nssv14582494
SamplesCHM13, CHM1, NA19240, HG00733
Known GenesCMIP
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)nsv3349098
Frequency
Sample Size14
Observed Gain0
Observed Loss4
Observed Complex0
Frequencyn/a


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