A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3361414



Internal ID19792392
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:10200391..10200576hg38UCSC Ensembl
chr2:10340517..10340702hg19UCSC Ensembl
Cytoband2p25.1
Allele length
AssemblyAllele length
hg38186
hg19186
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14614365, nssv14618739, nssv14623971, nssv14625814, nssv14618469, nssv14619172, nssv14622338, nssv14625927, nssv14628700
SamplesCHM13, HG02106, HG04217, CHM1, HG00268, HG02818, HX1, NA19434, NA19240
Known GenesC2orf48
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)nsv3361414
Frequency
Sample Size14
Observed Gain0
Observed Loss9
Observed Complex0
Frequencyn/a


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