A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3627047



Internal ID7013877
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:84425377..84519400hg38UCSC Ensembl
chr11:84136420..84230443hg19UCSC Ensembl
Cytoband11q14.1
Allele length
AssemblyAllele length
hg3894024
hg1994024
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv14220580, essv14220579, essv14220581
SamplesNA19036, HG01620, NA19430
Known GenesDLG2
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3627047
Frequency
Sample Size2504
Observed Gain0
Observed Loss3
Observed Complex0
Frequencyn/a


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