A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv10033n152



Internal ID22825736
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:11717222..11717813hg38UCSC Ensembl
chrX:11735342..11735933hg19UCSC Ensembl
CytobandXp22.2
Allele length
AssemblyAllele length
hg38592
hg19592
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv3198421, nsv3200941
SamplesNA19240
Known Genes
MethodMerging
Sequencing
AnalysisMultiple analysis algorthms
PhasedSV,MsPAC, Multiple Illumina callers, BioNano Genomics software
PlatformIllumina HiSeq
See merged experiments
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)dgv10033n152
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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