A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv800n152



Internal ID22816503
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:11282860..11285536hg38UCSC Ensembl
chr10:11324823..11327499hg19UCSC Ensembl
Cytoband10p14
Allele length
AssemblyAllele length
hg382677
hg192677
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv3203238, nsv3200637
SamplesNA19240, HG00514
Known GenesCELF2
MethodMerging
AnalysisPhasedSV,MsPAC, Multiple Illumina callers, BioNano Genomics software
PlatformSee merged experiments
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)dgv800n152
Frequency
Sample Size9
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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