A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3411476



Internal ID19842452
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:77725415..77725415hg38UCSC Ensembl
chr7:77354732..77354732hg19UCSC Ensembl
Cytoband7q11.23
Allele length
AssemblyAllele length
hg3858
hg1958
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14749122, nssv14733002, nssv14746323, nssv14744481, nssv14732927, nssv14742322, nssv14732677, nssv14734258
SamplesCHM13, HG04217, NA12878, HG02818, HX1, HG02059, NA19434, NA19240
Known GenesRSBN1L
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)nsv3411476
Frequency
Sample Size14
Observed Gain8
Observed Loss0
Observed Complex0
Frequencyn/a


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