A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14614277



Internal ID19204255
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:46297652..46297833hg38UCSC Ensembl
chr19:46800909..46801090hg19UCSC Ensembl
Cytoband19q13.32
Allele length
AssemblyAllele length
hg38182
hg19182
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3359900
Supporting Variants
SamplesHG02059
Known GenesHIF3A, RNU6-66P
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)nssv14614277
Frequency
Sample Size14
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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