A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14811979



Internal ID19226579
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:52516744..52516744hg38UCSC Ensembl
chrX:52545720..52545720hg19UCSC Ensembl
CytobandXp11.22
Allele length
AssemblyAllele length
hg3812871
hg1912871
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3410364
Supporting Variants
SamplesHG02059
Known GenesXAGE1A, XAGE1B, XAGE1C, XAGE1D, XAGE1E
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)nssv14811979
Frequency
Sample Size14
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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