A curated catalogue of human genomic structural variation




Variant Details

Variant: essv5931678



Internal ID8909081
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:131630103..131630635hg38UCSC Ensembl
chr11:131499997..131500529hg19UCSC Ensembl
Cytoband11q25
Allele length
AssemblyAllele length
hg38533
hg19533
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag1
Merged StatusS
Merged Variantsesv2666803
Supporting Variants
SamplesHG00662
Known GenesNTM
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)essv5931678
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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