A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3627196



Internal ID6667344
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:90231560..90283025hg38UCSC Ensembl
chr11:89964728..90016193hg19UCSC Ensembl
Cytoband11q14.3
Allele length
AssemblyAllele length
hg3851466
hg1951466
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv219e214
Supporting Variantsessv14231038, essv14231039
SamplesHG02561, HG00146
Known GenesDISC1FP1
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3627196
Frequency
Sample Size2504
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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