A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3387010



Internal ID19471302
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:159816141..159816141hg38UCSC Ensembl
chr6:160237173..160237173hg19UCSC Ensembl
Cytoband6q25.3
Allele length
AssemblyAllele length
hg38101
hg19101
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14747774, nssv14735383, nssv14736618, nssv14748344, nssv14749072, nssv14747003, nssv14746146, nssv14744933, nssv14744427, nssv14743144, nssv14742787, nssv14737984, nssv14732533, nssv14744608
SamplesCHM13, HG02106, HG04217, CHM1, HG00268, NA12878, HG02818, HX1, HG02059, HG01352, NA19434, NA19240, HG00733, HG00514
Known GenesPNLDC1
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)nsv3387010
Frequency
Sample Size14
Observed Gain14
Observed Loss0
Observed Complex0
Frequencyn/a


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