A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3409531



Internal ID19493821
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:14899115..14899115hg38UCSC Ensembl
chrX:14917237..14917237hg19UCSC Ensembl
CytobandXp22.2
Allele length
AssemblyAllele length
hg38346
hg19346
Variant TypeCNV alu insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14810482, nssv14792776, nssv14811517, nssv14810505
SamplesCHM13, HG04217, NA12878, HG00733
Known GenesMOSPD2
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)nsv3409531
Frequency
Sample Size14
Observed Gain4
Observed Loss0
Observed Complex0
Frequencyn/a


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