A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv10261n152



Internal ID22825964
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:120296566..120297171hg38UCSC Ensembl
chrX:119430421..119431026hg19UCSC Ensembl
CytobandXq24
Allele length
AssemblyAllele length
hg38606
hg19606
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv3525951, nsv3282666
SamplesNA19239, NA19240
Known GenesTMEM255A
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)dgv10261n152
Frequency
Sample Size9
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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