A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2666357



Internal ID9585776
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:118547983..118548600hg38UCSC Ensembl
chr11:118418698..118419315hg19UCSC Ensembl
Cytoband11q23.3
Allele length
AssemblyAllele length
hg38618
hg19618
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv6367111, essv5960178, essv5903375, essv5864958, essv6422783, essv6030756, essv6017258, essv5605249, essv5779586
SamplesHG00160, HG01082, HG01134, NA19463, NA19471, NA19444, HG01149, NA19468, NA18519
Known GenesIFT46
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)esv2666357
Frequency
Sample Size1151
Observed Gain0
Observed Loss9
Observed Complex0
Frequencyn/a


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