A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14792900



Internal ID19472307
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:34024874..34054733hg38UCSC Ensembl
chrX:34042991..34072850hg19UCSC Ensembl
CytobandXp21.1
Allele length
AssemblyAllele length
hg3829860
hg1929860
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3404892
Supporting Variants
SamplesHG00268
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)nssv14792900
Frequency
Sample Size14
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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