A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3628129



Internal ID6668273
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:132719968..132731213hg38UCSC Ensembl
Innerchr11:132720468..132730713hg38UCSC Ensembl
Outerchr11:132718968..132732213hg38UCSC Ensembl
chr11:132589863..132601108hg19UCSC Ensembl
Innerchr11:132590363..132600608hg19UCSC Ensembl
Outerchr11:132588863..132602108hg19UCSC Ensembl
Cytoband11q25
Allele length
AssemblyAllele length
hg3811246
hg1911246
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv14317693, essv14317694
SamplesNA20803, HG01595
Known GenesOPCML
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3628129
Frequency
Sample Size2504
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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