A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3628115



Internal ID6668259
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:132053654..132060279hg38UCSC Ensembl
chr11:131923548..131930173hg19UCSC Ensembl
Cytoband11q25
Allele length
AssemblyAllele length
hg386626
hg196626
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv14317179, essv14317180
SamplesNA20864, NA20886
Known GenesNTM
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3628115
Frequency
Sample Size2504
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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