A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3338092



Internal ID19769070
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:101067257..101067307hg38UCSC Ensembl
chr13:101719609..101719659hg19UCSC Ensembl
Cytoband13q33.1
Allele length
AssemblyAllele length
hg3851
hg1951
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14542401, nssv14532081, nssv14551481, nssv14542033
SamplesHG04217, HG02818, NA19434, HG00733
Known GenesNALCN
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)nsv3338092
Frequency
Sample Size14
Observed Gain0
Observed Loss4
Observed Complex0
Frequencyn/a


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