A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3627139



Internal ID7013969
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:88005218..88081249hg38UCSC Ensembl
chr11:87738386..87814417hg19UCSC Ensembl
Cytoband11q14.2
Allele length
AssemblyAllele length
hg3876032
hg1976032
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv217e214
Supporting Variantsessv14224073, essv14224072
SamplesHG01817, HG01807
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3627139
Frequency
Sample Size2504
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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