A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3626604



Internal ID7013436
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:62371957..62374720hg38UCSC Ensembl
Innerchr11:62371969..62374708hg38UCSC Ensembl
Outerchr11:62371945..62374732hg38UCSC Ensembl
chr11:62139429..62142192hg19UCSC Ensembl
Innerchr11:62139441..62142180hg19UCSC Ensembl
Outerchr11:62139417..62142204hg19UCSC Ensembl
Cytoband11q12.3
Allele length
AssemblyAllele length
hg382764
hg192764
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv14179386, essv14179385, essv14179388, essv14179383, essv14179384, essv14179387
SamplesHG03812, NA19704, HG00674, HG02545, NA19834, NA18628
Known GenesASRGL1
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3626604
Frequency
Sample Size2504
Observed Gain0
Observed Loss6
Observed Complex0
Frequencyn/a


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