A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv1363e199



Internal ID20124665
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:103000776..103061036hg38UCSC Ensembl
chr9:105763058..105823318hg19UCSC Ensembl
Cytoband9q31.1
Allele length
AssemblyAllele length
hg3860261
hg1960261
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsesv2669045, esv2663698
SamplesHG00375
Known GenesCYLC2
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)dgv1363e199
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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