A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv1378e199



Internal ID22759151
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:128429473..128434106hg38UCSC Ensembl
chr9:131191752..131196385hg19UCSC Ensembl
Cytoband9q34.11
Allele length
AssemblyAllele length
hg384634
hg194634
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsesv2665611, esv2669533
SamplesNA19472
Known GenesCERCAM
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)dgv1378e199
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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