A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3370324



Internal ID19454617
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:15162737..15162817hg38UCSC Ensembl
chr3:15204244..15204324hg19UCSC Ensembl
Cytoband3p25.1
Allele length
AssemblyAllele length
hg3881
hg1981
Variant TypeCNV mobile element deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14795059, nssv14805225
SamplesHG01352, NA19240
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
CommentsAbsence of a mobile element insertion that is present in the reference
ReferenceAudano_et_al_2019
Pubmed ID30661756
Accession Number(s)nsv3370324
Frequency
Sample Size14
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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