A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3379764



Internal ID19464056
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:109835690..109835833hg38UCSC Ensembl
chr4:110756846..110756989hg19UCSC Ensembl
Cytoband4q25
Allele length
AssemblyAllele length
hg38144
hg19144
Variant TypeCNV mobile element deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14809729
SamplesHG04217
Known GenesRRH
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
CommentsAbsence of a mobile element insertion that is present in the reference
ReferenceAudano_et_al_2019
Pubmed ID30661756
Accession Number(s)nsv3379764
Frequency
Sample Size14
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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