A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3388584



Internal ID19819561
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:46779377..46779377hg38UCSC Ensembl
chr6:46747114..46747114hg19UCSC Ensembl
Cytoband6p12.3
Allele length
AssemblyAllele length
hg38538
hg19538
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14717721
SamplesCHM1
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)nsv3388584
Frequency
Sample Size14
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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