A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2667097



Internal ID9933202
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:6409642..6409837hg38UCSC Ensembl
chr11:6430872..6431067hg19UCSC Ensembl
Cytoband11p15.4
Allele length
AssemblyAllele length
hg38196
hg19196
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv5493819, essv5618486, essv6407796, essv5908769, essv6420475, essv6470918, essv6237966, essv6007492, essv6179142, essv6366640, essv6347607, essv5771721, essv6218505
SamplesNA18508, NA18498, NA18520, NA19663, NA18499, NA18853, NA19225, NA18909, NA20281, NA18501, NA19093, NA19102, NA18505
Known GenesAPBB1
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)esv2667097
Frequency
Sample Size1151
Observed Gain0
Observed Loss13
Observed Complex0
Frequencyn/a


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