A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3626055



Internal ID7012889
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:40014842..40020300hg38UCSC Ensembl
Innerchr11:40014842..40020300hg38UCSC Ensembl
Outerchr11:40014577..40020547hg38UCSC Ensembl
chr11:40036392..40041850hg19UCSC Ensembl
Innerchr11:40036392..40041850hg19UCSC Ensembl
Outerchr11:40036127..40042097hg19UCSC Ensembl
Cytoband11p12
Allele length
AssemblyAllele length
hg385459
hg195459
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv14103194, essv14103193
SamplesNA18547, NA18573
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3626055
Frequency
Sample Size2504
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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