A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2656592



Internal ID9922697
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:133495690..133496082hg38UCSC Ensembl
chr9:136360812..136361204hg19UCSC Ensembl
Cytoband9q34.2
Allele length
AssemblyAllele length
hg38393
hg19393
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv1384e199
Supporting Variantsessv5425493, essv6517589, essv6579313, essv5414382, essv5955275, essv5798203, essv6131550, essv6236819, essv5422262, essv6574517, essv5818204, essv5412875, essv6270903, essv6298606, essv5480958, essv6016872, essv5767366, essv6463472, essv6119058, essv6019215, essv5566753, essv5991282, essv6559079
SamplesNA12717, NA12842, NA20783, NA12843, NA20507, NA12413, NA20537, NA20796, NA12889, NA20811, NA12748, NA18951, NA20800, NA20787, NA20760, NA12829, NA20773, NA20778, NA20803, NA20797, NA20786, NA20503, NA12890
Known Genes
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)esv2656592
Frequency
Sample Size1151
Observed Gain0
Observed Loss23
Observed Complex0
Frequencyn/a


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