A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3626599



Internal ID6666749
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:62325417..62389620hg38UCSC Ensembl
Innerchr11:62325567..62389470hg38UCSC Ensembl
Outerchr11:62325267..62389770hg38UCSC Ensembl
chr11:62092889..62157092hg19UCSC Ensembl
Innerchr11:62093039..62156942hg19UCSC Ensembl
Outerchr11:62092739..62157242hg19UCSC Ensembl
Cytoband11q12.3
Allele length
AssemblyAllele length
hg3864204
hg1964204
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv14179361, essv14179363, essv14179364, essv14179362, essv14179360
SamplesHG00142, HG03363, HG02256, HG02772, HG03470
Known GenesASRGL1
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3626599
Frequency
Sample Size2504
Observed Gain5
Observed Loss0
Observed Complex0
Frequencyn/a


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