A curated catalogue of human genomic structural variation




Variant Details

Variant: essv14221298



Internal ID5941086
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:85406079..85573925hg38UCSC Ensembl
chr11:85117123..85284969hg19UCSC Ensembl
Cytoband11q14.1
Allele length
AssemblyAllele length
hg38167847
hg19167847
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3627063
Supporting Variants
SamplesNA19351
Known GenesDLG2
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv14221298
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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