A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2670316



Internal ID9936421
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:127406971..127409927hg38UCSC Ensembl
Outerchr11:127406250..127410647hg38UCSC Ensembl
Innerchr11:127276866..127279822hg19UCSC Ensembl
Outerchr11:127276145..127280542hg19UCSC Ensembl
Cytoband11q24.2
Allele length
AssemblyAllele length
hg384398
hg194398
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv249e199
Supporting Variantsessv6102671, essv6176081, essv5639087, essv6362842, essv6199487, essv5623101, essv5708407, essv6329770, essv5980961, essv6324242, essv6188233, essv6441319, essv6045071, essv6113244, essv5517547, essv6256251, essv6467204, essv6591353, essv5480924
SamplesNA19443, NA19190, NA19130, NA19189, NA19445, NA19455, NA19449, NA19453, NA19452, NA19321, NA19434, NA19473, NA19470, NA19467, NA19468, NA19102, NA19312, NA18522, NA19429
Known Genes
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)esv2670316
Frequency
Sample Size1151
Observed Gain0
Observed Loss19
Observed Complex0
Frequencyn/a


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