A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3627338



Internal ID7014168
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:95150469..95151034hg38UCSC Ensembl
Innerchr11:95150470..95151034hg38UCSC Ensembl
Outerchr11:95150469..95151035hg38UCSC Ensembl
chr11:94883633..94884198hg19UCSC Ensembl
Innerchr11:94883634..94884198hg19UCSC Ensembl
Outerchr11:94883633..94884199hg19UCSC Ensembl
Cytoband11q21
Allele length
AssemblyAllele length
hg38566
hg19566
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv14243293, essv14243290, essv14243280, essv14243267, essv14243282, essv14243277, essv14243296, essv14243276, essv14243270, essv14243286, essv14243269, essv14243279, essv14243268, essv14243292, essv14243287, essv14243266, essv14243273, essv14243284, essv14243288, essv14243281, essv14243278, essv14243272, essv14243289, essv14243274, essv14243264, essv14243295, essv14243271, essv14243285, essv14243291, essv14243283, essv14243265, essv14243294, essv14243275
SamplesHG00235, NA19028, NA19700, NA20766, HG03052, NA18507, HG02836, HG03558, HG02325, HG02860, HG02562, NA19235, HG02545, HG02882, HG03369, NA19027, HG03363, HG03511, NA19347, HG01684, HG03457, HG03428, HG03567, HG02813, NA19149, HG02721, HG01272, NA19380, NA20362, NA19475, NA19474, HG02052, HG02763
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3627338
Frequency
Sample Size2504
Observed Gain0
Observed Loss33
Observed Complex0
Frequencyn/a


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