A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2656536



Internal ID9922641
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:60683572..60684261hg38UCSC Ensembl
chr11:60451045..60451734hg19UCSC Ensembl
Cytoband11q12.2
Allele length
AssemblyAllele length
hg38690
hg19690
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv5741420, essv6234303, essv5922492, essv6537386
SamplesHG00143, NA12342, HG00344, NA12154
Known GenesLINC00301
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
CommentsHigh quality site
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)esv2656536
Frequency
Sample Size1151
Observed Gain0
Observed Loss4
Observed Complex0
Frequencyn/a


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