A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv10270n152



Internal ID22825973
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:123550665..123550825hg38UCSC Ensembl
chrX:122684516..122684676hg19UCSC Ensembl
CytobandXq25
Allele length
AssemblyAllele length
hg38161
hg19161
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv3194280, nsv3201830
SamplesHG00512, HG00514
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)dgv10270n152
Frequency
Sample Size9
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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