A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv1024n152



Internal ID22816727
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:98407737..98407796hg38UCSC Ensembl
chr10:100167494..100167553hg19UCSC Ensembl
Cytoband10q24.2
Allele length
AssemblyAllele length
hg3860
hg1960
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv3218458, nsv3212649
SamplesHG00731, HG00733, HG00513, HG00514
Known GenesPYROXD2
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)dgv1024n152
Frequency
Sample Size9
Observed Gain0
Observed Loss4
Observed Complex0
Frequencyn/a


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