A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3626602



Internal ID7013434
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:62366666..62381581hg38UCSC Ensembl
chr11:62134138..62149053hg19UCSC Ensembl
Cytoband11q12.3
Allele length
AssemblyAllele length
hg3814916
hg1914916
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv202e214
Supporting Variantsessv14179376, essv14179375, essv14179373, essv14179374
SamplesNA19704, HG00674, HG02545, NA19834
Known GenesASRGL1
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3626602
Frequency
Sample Size2504
Observed Gain0
Observed Loss4
Observed Complex0
Frequencyn/a


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