A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3349371



Internal ID19780349
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:15363354..15363482hg38UCSC Ensembl
chr19:15474165..15474293hg19UCSC Ensembl
Cytoband19p13.12
Allele length
AssemblyAllele length
hg38129
hg19129
Variant TypeCNV sva deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14812412
SamplesHG00268
Known GenesAKAP8
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 SVA insertion that is present in the reference
ReferenceAudano_et_al_2019
Pubmed ID30661756
Accession Number(s)nsv3349371
Frequency
Sample Size14
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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