A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3377969



Internal ID19808947
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:55266505..55266505hg38UCSC Ensembl
chr19:55777873..55777873hg19UCSC Ensembl
Cytoband19q13.42
Allele length
AssemblyAllele length
hg38310
hg19310
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14627062, nssv14623928, nssv14619579, nssv14617217, nssv14626699, nssv14621936, nssv14631146, nssv14629004, nssv14618655, nssv14627809
SamplesCHM13, CHM1, NA12878, HG02818, HX1, HG02059, HG01352, NA19434, NA19240, HG00733
Known GenesHSPBP1
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)nsv3377969
Frequency
Sample Size14
Observed Gain10
Observed Loss0
Observed Complex0
Frequencyn/a


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