A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3351682



Internal ID19782660
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:30839196..30839552hg38UCSC Ensembl
chr13:31413333..31413689hg19UCSC Ensembl
Cytoband13q12.3
Allele length
AssemblyAllele length
hg38357
hg19357
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14548156, nssv14539048, nssv14533533, nssv14533096, nssv14551999
SamplesHX1, HG02059, HG01352, HG00733, HG00514
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)nsv3351682
Frequency
Sample Size14
Observed Gain0
Observed Loss5
Observed Complex0
Frequencyn/a


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