A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3381560



Internal ID19465853
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:38561817..38561879hg38UCSC Ensembl
chr3:38603308..38603370hg19UCSC Ensembl
Cytoband3p22.2
Allele length
AssemblyAllele length
hg3863
hg1963
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14664287, nssv14662258, nssv14665206, nssv14671604, nssv14658071, nssv14663555
SamplesCHM1, HG02818, HX1, NA19434, NA19240, HG00514
Known GenesSCN5A
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)nsv3381560
Frequency
Sample Size14
Observed Gain0
Observed Loss6
Observed Complex0
Frequencyn/a


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