A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3627247



Internal ID7014077
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:91482412..91483607hg38UCSC Ensembl
Innerchr11:91482425..91483595hg38UCSC Ensembl
Outerchr11:91482400..91483620hg38UCSC Ensembl
chr11:91215578..91216773hg19UCSC Ensembl
Innerchr11:91215591..91216761hg19UCSC Ensembl
Outerchr11:91215566..91216786hg19UCSC Ensembl
Cytoband11q14.3
Allele length
AssemblyAllele length
hg381196
hg191196
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv14233443, essv14233441, essv14233442, essv14233445, essv14233444, essv14233440, essv14233446
SamplesHG03096, HG03484, NA19393, HG03478, HG03394, HG03469, HG03565
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3627247
Frequency
Sample Size2504
Observed Gain0
Observed Loss7
Observed Complex0
Frequencyn/a


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