A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv10298n152



Internal ID22826001
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:135374593..135403747hg38UCSC Ensembl
chrX:134508518..134537672hg19UCSC Ensembl
CytobandXq26.3
Allele length
AssemblyAllele length
hg3829155
hg1929155
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv3194963, nsv3190668
SamplesNA19239, NA19240
Known GenesLOC100506790
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)dgv10298n152
Frequency
Sample Size9
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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