A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3626696



Internal ID7013527
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:66552406..66562756hg38UCSC Ensembl
Innerchr11:66552406..66562756hg38UCSC Ensembl
Outerchr11:66552172..66563011hg38UCSC Ensembl
chr11:66319877..66330227hg19UCSC Ensembl
Innerchr11:66319877..66330227hg19UCSC Ensembl
Outerchr11:66319643..66330482hg19UCSC Ensembl
Cytoband11q13.2
Allele length
AssemblyAllele length
hg3810351
hg1910351
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv14195777, essv14195774, essv14195778, essv14195776, essv14195775, essv14195779
SamplesHG01853, HG02178, HG02402, HG02070, HG01878, HG02401
Known GenesACTN3
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3626696
Frequency
Sample Size2504
Observed Gain0
Observed Loss6
Observed Complex0
Frequencyn/a


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