A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3334634



Internal ID19765612
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:121747794..121747794hg38UCSC Ensembl
chr12:122185700..122185700hg19UCSC Ensembl
Cytoband12q24.31
Allele length
AssemblyAllele length
hg38798
hg19798
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14546834, nssv14540106, nssv14541892, nssv14534831, nssv14533818
SamplesCHM13, HG02106, HG00268, NA12878, HG02059
Known GenesTMEM120B
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)nsv3334634
Frequency
Sample Size14
Observed Gain5
Observed Loss0
Observed Complex0
Frequencyn/a


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