A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14798218



Internal ID19198521
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:24709160..24709160hg38UCSC Ensembl
chrX:24727277..24727277hg19UCSC Ensembl
CytobandXp22.11
Allele length
AssemblyAllele length
hg38128
hg19128
Variant TypeCNV sva insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3402977
Supporting Variants
SamplesHG01352
Known GenesPOLA1
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)nssv14798218
Frequency
Sample Size14
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer