A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3416460



Internal ID19500749
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:55120514..55120514hg38UCSC Ensembl
chr8:56033074..56033074hg19UCSC Ensembl
Cytoband8q12.1
Allele length
AssemblyAllele length
hg38341
hg19341
Variant TypeCNV alu insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14754844, nssv14762303, nssv14767505
SamplesCHM1, HX1, NA19434
Known GenesXKR4
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)nsv3416460
Frequency
Sample Size14
Observed Gain3
Observed Loss0
Observed Complex0
Frequencyn/a


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