A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3626676



Internal ID7013508
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:65683808..65687363hg38UCSC Ensembl
Innerchr11:65684308..65686863hg38UCSC Ensembl
Outerchr11:65682808..65688363hg38UCSC Ensembl
chr11:65451279..65454834hg19UCSC Ensembl
Innerchr11:65451779..65454334hg19UCSC Ensembl
Outerchr11:65450279..65455834hg19UCSC Ensembl
Cytoband11q13.1
Allele length
AssemblyAllele length
hg383556
hg193556
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv14189794, essv14189793
SamplesNA19350, NA19023
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3626676
Frequency
Sample Size2504
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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