A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14482049



Internal ID19178477
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:149431701..149461600hg38UCSC Ensembl
chr1:145249580..145279474hg19UCSC Ensembl
Cytoband1q21.1
Allele length
AssemblyAllele length
hg3829900
hg1929895
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3320603
Supporting Variants
SamplesHG01352
Known GenesLOC100288142, NBPF9, NOTCH2NL
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)nssv14482049
Frequency
Sample Size14
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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