A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14649062



Internal ID19190473
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:34560261..34560410hg38UCSC Ensembl
chr20:33148065..33148214hg19UCSC Ensembl
Cytoband20q11.22
Allele length
AssemblyAllele length
hg38150
hg19150
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3378410
Supporting Variants
SamplesHG01352
Known GenesMAP1LC3A
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)nssv14649062
Frequency
Sample Size14
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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