A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3627399



Internal ID7014228
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:97191702..97353386hg38UCSC Ensembl
chr11:97062702..97224386hg19UCSC Ensembl
Cytoband11q21
Allele length
AssemblyAllele length
hg38161685
hg19161685
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv14245469, essv14245468
SamplesNA18988, NA20334
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3627399
Frequency
Sample Size2504
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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