A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3628112



Internal ID6668256
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:131849751..131854665hg38UCSC Ensembl
Innerchr11:131849751..131854665hg38UCSC Ensembl
Outerchr11:131849510..131854946hg38UCSC Ensembl
chr11:131719645..131724559hg19UCSC Ensembl
Innerchr11:131719645..131724559hg19UCSC Ensembl
Outerchr11:131719404..131724840hg19UCSC Ensembl
Cytoband11q25
Allele length
AssemblyAllele length
hg384915
hg194915
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv14317096, essv14317093, essv14317094, essv14317095
SamplesHG02356, HG00701, HG02379, NA18562
Known GenesNTM
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3628112
Frequency
Sample Size2504
Observed Gain0
Observed Loss4
Observed Complex0
Frequencyn/a


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