A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2666119



Internal ID9932224
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:114938105..114949754hg38UCSC Ensembl
chr3:114656952..114668601hg19UCSC Ensembl
Cytoband3q13.31
Allele length
AssemblyAllele length
hg3811650
hg1911650
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv881e199
Supporting Variantsessv6544645, essv6302842, essv6402944, essv6070287, essv6491376, essv5446457, essv5577344
SamplesNA19371, NA19390, NA19360, NA19078, NA18873, NA19213, NA19463
Known GenesZBTB20
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)esv2666119
Frequency
Sample Size1151
Observed Gain0
Observed Loss7
Observed Complex0
Frequencyn/a


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