A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv1090n152



Internal ID22816793
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:124471440..124475040hg38UCSC Ensembl
chr10:126160009..126163609hg19UCSC Ensembl
Cytoband10q26.13
Allele length
AssemblyAllele length
hg383601
hg193601
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv3230112, nsv3224564
SamplesNA19239, NA19240
Known GenesLHPP
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)dgv1090n152
Frequency
Sample Size9
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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