A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3626635



Internal ID7013467
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:63418984..63432304hg38UCSC Ensembl
chr11:63186456..63199776hg19UCSC Ensembl
Cytoband11q12.3
Allele length
AssemblyAllele length
hg3813321
hg1913321
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv14182618
SamplesHG02150
Known GenesMIR3680-1, MIR3680-2
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3626635
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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