A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv824n152



Internal ID22816527
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:18741447..18741602hg38UCSC Ensembl
chr10:19030376..19030531hg19UCSC Ensembl
Cytoband10p12.31
Allele length
AssemblyAllele length
hg38156
hg19156
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv3285457, nsv3220537
SamplesNA19238, NA19240, HG00733
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)dgv824n152
Frequency
Sample Size9
Observed Gain0
Observed Loss3
Observed Complex0
Frequencyn/a


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