A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv10300n152



Internal ID22826003
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:135713409..135815598hg38UCSC Ensembl
Cytoband
Allele length
AssemblyAllele length
hg38102190
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv3198067, nsv3196165
SamplesHG00733
Known Genes
MethodMerging
Optical mapping
AnalysisBioNano Genomics proprietary analysis
PhasedSV,MsPAC, Multiple Illumina callers, BioNano Genomics software
PlatformBioNano Genomics
See merged experiments
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)dgv10300n152
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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