A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3326714



Internal ID19757692
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:114253209..114253209hg38UCSC Ensembl
chr10:116012968..116012968hg19UCSC Ensembl
Cytoband10q25.3
Allele length
AssemblyAllele length
hg38146
hg19146
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14494952, nssv14509411, nssv14497487, nssv14495413
SamplesHG02106, HG04217, HG02059, HG00514
Known GenesVWA2
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)nsv3326714
Frequency
Sample Size14
Observed Gain4
Observed Loss0
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer