A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2671960



Internal ID9591379
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:43197208..43197645hg38UCSC Ensembl
chr6:43164946..43165383hg19UCSC Ensembl
Cytoband6p21.1
Allele length
AssemblyAllele length
hg38438
hg19438
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv6016793, essv5426494, essv5513935, essv6478198, essv6044252, essv5790222
SamplesNA19436, NA19401, NA19453, NA19434, NA19448, NA19385
Known GenesCUL9
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)esv2671960
Frequency
Sample Size1151
Observed Gain0
Observed Loss6
Observed Complex0
Frequencyn/a


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