A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv2547n152



Internal ID22818250
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:21588033..21597991hg38UCSC Ensembl
chr14:22056152..22066116hg19UCSC Ensembl
Cytoband14q11.2
Allele length
AssemblyAllele length
hg389959
hg199965
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv3202483, nsv3201978
SamplesNA19240
Known Genes
MethodMerging
AnalysisPhasedSV,MsPAC, Multiple Illumina callers, BioNano Genomics software
PlatformSee merged experiments
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)dgv2547n152
Frequency
Sample Size9
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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