A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv1350e199



Internal ID22759123
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:64723746..65207445hg38UCSC Ensembl
chr9:69736164..70101051hg19UCSC Ensembl
Cytoband9q21.11
Allele length
AssemblyAllele length
hg38483700
hg19364888
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsesv2677134, esv2661574
SamplesHG00149, HG00190
Known Genes
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)dgv1350e199
Frequency
Sample Size1151
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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