A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3627989



Internal ID6668133
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:124811876..124812891hg38UCSC Ensembl
Innerchr11:124811877..124812890hg38UCSC Ensembl
Outerchr11:124811875..124812892hg38UCSC Ensembl
chr11:124681772..124682787hg19UCSC Ensembl
Innerchr11:124681773..124682786hg19UCSC Ensembl
Outerchr11:124681771..124682788hg19UCSC Ensembl
Cytoband11q24.2
Allele length
AssemblyAllele length
hg381016
hg191016
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv14302226, essv14302219, essv14302227, essv14302237, essv14302212, essv14302213, essv14302238, essv14302234, essv14302236, essv14302239, essv14302230, essv14302232, essv14302218, essv14302240, essv14302228, essv14302214, essv14302220, essv14302224, essv14302241, essv14302233, essv14302229, essv14302221, essv14302223, essv14302225, essv14302217, essv14302222, essv14302231, essv14302235, essv14302215, essv14302216
SamplesNA19141, HG03297, HG03193, NA20356, HG03069, HG03074, NA19171, HG02840, HG03246, NA19372, HG01312, HG02570, HG02537, HG01889, NA18907, HG03311, HG03123, HG03388, HG03046, HG02722, HG02330, NA20276, HG03419, HG03112, HG03049, HG02465, HG01886, HG02643, HG02006, HG01191
Known GenesLOC100507283
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3627989
Frequency
Sample Size2504
Observed Gain0
Observed Loss30
Observed Complex0
Frequencyn/a


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