A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv823n152



Internal ID22816526
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:18561028..18561399hg38UCSC Ensembl
chr10:18849957..18850328hg19UCSC Ensembl
Cytoband10p12.31
Allele length
AssemblyAllele length
hg38372
hg19372
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv3284731, nsv3288556, nsv3287171
SamplesNA19240, HG00733, HG00514
Known GenesNSUN6
MethodMerging
AnalysisPhasedSV,MsPAC, Multiple Illumina callers, BioNano Genomics software
PlatformSee merged experiments
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)dgv823n152
Frequency
Sample Size9
Observed Gain0
Observed Loss3
Observed Complex0
Frequencyn/a


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