A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14510066



Internal ID19670918
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:101855065..101855065hg38UCSC Ensembl
chr10:103614822..103614822hg19UCSC Ensembl
Cytoband10q24.32
Allele length
AssemblyAllele length
hg381513
hg191513
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3326669
Supporting Variants
SamplesHX1
Known GenesC10orf76
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)nssv14510066
Frequency
Sample Size14
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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