A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3628113



Internal ID6668257
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:131917641..131921538hg38UCSC Ensembl
Innerchr11:131917653..131921526hg38UCSC Ensembl
Outerchr11:131917629..131921550hg38UCSC Ensembl
chr11:131787535..131791432hg19UCSC Ensembl
Innerchr11:131787547..131791420hg19UCSC Ensembl
Outerchr11:131787523..131791444hg19UCSC Ensembl
Cytoband11q25
Allele length
AssemblyAllele length
hg383898
hg193898
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv14317097
SamplesNA20813
Known GenesNTM
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3628113
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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