A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3627344



Internal ID7014174
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:95309415..95313698hg38UCSC Ensembl
Innerchr11:95309416..95313697hg38UCSC Ensembl
Outerchr11:95309414..95313699hg38UCSC Ensembl
chr11:95042579..95046862hg19UCSC Ensembl
Innerchr11:95042580..95046861hg19UCSC Ensembl
Outerchr11:95042578..95046863hg19UCSC Ensembl
Cytoband11q21
Allele length
AssemblyAllele length
hg384284
hg194284
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv14243447, essv14243452, essv14243442, essv14243457, essv14243439, essv14243449, essv14243445, essv14243453, essv14243443, essv14243448, essv14243444, essv14243454, essv14243451, essv14243446, essv14243455, essv14243440, essv14243450, essv14243456, essv14243441
SamplesHG04210, HG03753, HG03679, NA19068, HG03754, HG03911, HG03793, NA18986, HG03007, NA18516, HG03730, NA19000, HG03991, HG03778, HG03899, NA19331, NA19334, HG03733, HG04061
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3627344
Frequency
Sample Size2504
Observed Gain0
Observed Loss19
Observed Complex0
Frequencyn/a


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