A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14618194



Internal ID19672290
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:54959209..54960665hg38UCSC Ensembl
chr19:55470577..55472033hg19UCSC Ensembl
Cytoband19q13.42
Allele length
AssemblyAllele length
hg381457
hg191457
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3364664
Supporting Variants
SamplesNA12878
Known GenesRNU6-35P, RNU6-64P
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)nssv14618194
Frequency
Sample Size14
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer