A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv1011n152



Internal ID22816714
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:91209461..91209806hg38UCSC Ensembl
chr10:92969218..92969563hg19UCSC Ensembl
Cytoband10q23.32
Allele length
AssemblyAllele length
hg38346
hg19346
Variant TypeCNV alu deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv3520672, nsv3188770
SamplesHG00512, NA19238, NA19239, HG00731, HG00732, NA19240, HG00733, HG00513, HG00514
Known GenesPCGF5
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)dgv1011n152
Frequency
Sample Size9
Observed Gain0
Observed Loss9
Observed Complex0
Frequencyn/a


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