A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3627956



Internal ID7014781
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:123444017..123449868hg38UCSC Ensembl
Innerchr11:123444017..123449868hg38UCSC Ensembl
Outerchr11:123443731..123450097hg38UCSC Ensembl
chr11:123314725..123320576hg19UCSC Ensembl
Innerchr11:123314725..123320576hg19UCSC Ensembl
Outerchr11:123314439..123320805hg19UCSC Ensembl
Cytoband11q24.1
Allele length
AssemblyAllele length
hg385852
hg195852
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv14301205, essv14301206, essv14301207, essv14301211, essv14301210, essv14301208, essv14301203, essv14301209, essv14301213, essv14301201, essv14301204, essv14301212, essv14301202
SamplesNA18641, HG00452, HG00674, HG01816, HG00543, HG02402, HG02152, NA18939, HG00500, HG00704, NA18541, HG00623, HG03611
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3627956
Frequency
Sample Size2504
Observed Gain0
Observed Loss13
Observed Complex0
Frequencyn/a


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