A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv10089n152



Internal ID22825792
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:40046522..40046576hg38UCSC Ensembl
chrX:39905775..39905829hg19UCSC Ensembl
CytobandXp11.4
Allele length
AssemblyAllele length
hg3855
hg1955
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv3206773, nsv3195672
SamplesNA19238, NA19239, NA19240
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)dgv10089n152
Frequency
Sample Size9
Observed Gain0
Observed Loss3
Observed Complex0
Frequencyn/a


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