A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv2556n152



Internal ID22818259
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:23939282..23939483hg38UCSC Ensembl
chr14:24408491..24408692hg19UCSC Ensembl
Cytoband14q11.2
Allele length
AssemblyAllele length
hg38202
hg19202
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv3195438, nsv3196667
SamplesNA19240, HG00733
Known GenesDHRS4-AS1
MethodMerging
AnalysisPhasedSV,MsPAC, Multiple Illumina callers, BioNano Genomics software
PlatformSee merged experiments
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)dgv2556n152
Frequency
Sample Size9
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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