A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3627884



Internal ID7014709
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:119038560..119041729hg38UCSC Ensembl
Innerchr11:119038586..119041704hg38UCSC Ensembl
Outerchr11:119038535..119041755hg38UCSC Ensembl
chr11:118909270..118912439hg19UCSC Ensembl
Innerchr11:118909296..118912414hg19UCSC Ensembl
Outerchr11:118909245..118912465hg19UCSC Ensembl
Cytoband11q23.3
Allele length
AssemblyAllele length
hg383170
hg193170
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv14293304, essv14293302, essv14293305, essv14293303
SamplesNA12842, NA12414, HG01500, HG01626
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3627884
Frequency
Sample Size2504
Observed Gain0
Observed Loss4
Observed Complex0
Frequencyn/a


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