A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3626717



Internal ID6666865
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:67677103..67677881hg38UCSC Ensembl
Innerchr11:67677153..67677831hg38UCSC Ensembl
Outerchr11:67677026..67677958hg38UCSC Ensembl
chr11:67444574..67445352hg19UCSC Ensembl
Innerchr11:67444624..67445302hg19UCSC Ensembl
Outerchr11:67444497..67445429hg19UCSC Ensembl
Cytoband11q13.2
Allele length
AssemblyAllele length
hg38779
hg19779
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv14198393, essv14198394, essv14198395, essv14198392
SamplesHG03120, NA19256, HG02501, NA18499
Known GenesALDH3B2
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3626717
Frequency
Sample Size2504
Observed Gain0
Observed Loss4
Observed Complex0
Frequencyn/a


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