A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3321188



Internal ID19752166
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:17683146..17683313hg38UCSC Ensembl
chr1:18009641..18009808hg19UCSC Ensembl
Cytoband1p36.13
Allele length
AssemblyAllele length
hg38168
hg19168
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14490712, nssv14491667, nssv14479991, nssv14474738
SamplesCHM1, HG02059, NA19434, HG00733
Known GenesARHGEF10L
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)nsv3321188
Frequency
Sample Size14
Observed Gain0
Observed Loss4
Observed Complex0
Frequencyn/a


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