A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3627899



Internal ID6668043
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:120129619..120131730hg38UCSC Ensembl
Innerchr11:120129619..120131730hg38UCSC Ensembl
Outerchr11:120129327..120132006hg38UCSC Ensembl
chr11:120000327..120002438hg19UCSC Ensembl
Innerchr11:120000327..120002438hg19UCSC Ensembl
Outerchr11:120000035..120002714hg19UCSC Ensembl
Cytoband11q23.3
Allele length
AssemblyAllele length
hg382112
hg192112
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv14294707, essv14294709, essv14294702, essv14294705, essv14294703, essv14294710, essv14294708, essv14294704, essv14294706
SamplesHG02697, HG01777, HG00581, NA20849, HG00239, HG03944, HG01676, HG04212, HG01630
Known GenesTRIM29
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3627899
Frequency
Sample Size2504
Observed Gain0
Observed Loss9
Observed Complex0
Frequencyn/a


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