A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2662833



Internal ID9928938
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:33993274..33996500hg38UCSC Ensembl
chr11:34014821..34018047hg19UCSC Ensembl
Cytoband11p13
Allele length
AssemblyAllele length
hg383227
hg193227
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv6267429, essv5425618, essv6071091, essv6589344, essv6526496, essv5972955, essv6202216, essv5460679, essv5499525, essv5921031, essv5732041, essv6271815, essv6037273, essv6382836, essv5585288, essv6296399, essv5737436, essv5421692, essv6460853, essv6226188
SamplesNA19394, NA19909, HG00640, NA19355, NA20346, NA19384, NA19404, NA19383, NA19901, NA19445, NA19437, NA19707, NA19403, NA18933, NA18907, NA19099, NA19428, NA19468, NA19900, HG01125
Known Genes
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
CommentsHigh quality site
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)esv2662833
Frequency
Sample Size1151
Observed Gain0
Observed Loss20
Observed Complex0
Frequencyn/a


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