A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3374553



Internal ID19805531
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:21305488..21308169hg38UCSC Ensembl
chr20:21286126..21288807hg19UCSC Ensembl
Cytoband20p11.23
Allele length
AssemblyAllele length
hg382682
hg192682
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14641590, nssv14649850, nssv14648999, nssv14639901, nssv14645563, nssv14647718, nssv14636862, nssv14650962, nssv14638480, nssv14637423, nssv14650782, nssv14651440, nssv14639906
SamplesCHM13, HG02106, HG04217, CHM1, HG00268, HG02818, HX1, HG02059, HG01352, NA19434, NA19240, HG00733, HG00514
Known GenesXRN2
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)nsv3374553
Frequency
Sample Size14
Observed Gain0
Observed Loss13
Observed Complex0
Frequencyn/a


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