A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3321995



Internal ID19406287
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:205981655..205981794hg38UCSC Ensembl
Cytoband
Allele length
AssemblyAllele length
hg38140
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14475386, nssv14489952, nssv14488029, nssv14480347, nssv14487030, nssv14485728, nssv14475274, nssv14482486, nssv14478163
SamplesCHM13, HG02106, CHM1, HG00268, NA12878, HG02818, HX1, HG00733, HG00514
Known Genes
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)nsv3321995
Frequency
Sample Size14
Observed Gain0
Observed Loss9
Observed Complex0
Frequencyn/a


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