A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3628003



Internal ID6668147
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:126314394..126317250hg38UCSC Ensembl
Innerchr11:126314398..126317246hg38UCSC Ensembl
Outerchr11:126314390..126317254hg38UCSC Ensembl
chr11:126184289..126187145hg19UCSC Ensembl
Innerchr11:126184293..126187141hg19UCSC Ensembl
Outerchr11:126184285..126187149hg19UCSC Ensembl
Cytoband11q24.2
Allele length
AssemblyAllele length
hg382857
hg192857
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv14302950, essv14302957, essv14302955, essv14302959, essv14302951, essv14302961, essv14302958, essv14302953, essv14302963, essv14302954, essv14302962, essv14302964, essv14302952, essv14302960, essv14302956, essv14302949
SamplesHG03298, NA19916, HG02111, HG03268, NA19024, NA19235, HG02442, HG02508, HG03311, HG03117, NA19360, HG02558, NA20348, HG02974, HG03445, NA19346
Known GenesDCPS
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3628003
Frequency
Sample Size2504
Observed Gain0
Observed Loss16
Observed Complex0
Frequencyn/a


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