A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3385069



Internal ID19816047
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:34098601..34126600hg38UCSC Ensembl
chr5:34098706..34126705hg19UCSC Ensembl
Cytoband5p13.2
Allele length
AssemblyAllele length
hg3828000
hg1928000
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14702198, nssv14693951, nssv14697352
SamplesHG04217, NA12878, NA19434
Known GenesC1QTNF3-AMACR
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)nsv3385069
Frequency
Sample Size14
Observed Gain3
Observed Loss0
Observed Complex0
Frequencyn/a


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