A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3627985



Internal ID6668129
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:124662251..124669278hg38UCSC Ensembl
Innerchr11:124662251..124669278hg38UCSC Ensembl
Outerchr11:124661968..124669536hg38UCSC Ensembl
chr11:124532147..124539174hg19UCSC Ensembl
Innerchr11:124532147..124539174hg19UCSC Ensembl
Outerchr11:124531864..124539432hg19UCSC Ensembl
Cytoband11q24.2
Allele length
AssemblyAllele length
hg387028
hg197028
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv14302142
SamplesNA19467
Known GenesSIAE
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3627985
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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