A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv237e214



Internal ID18980412
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:133063637..133101272hg38UCSC Ensembl
chr11:132933532..132971167hg19UCSC Ensembl
Cytoband11q25
Allele length
AssemblyAllele length
hg3837636
hg1937636
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsesv3628136, esv3628137
SamplesHG01308
Known GenesOPCML
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)dgv237e214
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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