A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3626866



Internal ID7013696
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:76256314..76258958hg38UCSC Ensembl
Innerchr11:76256364..76258908hg38UCSC Ensembl
Outerchr11:76256264..76259008hg38UCSC Ensembl
chr11:75967358..75970002hg19UCSC Ensembl
Innerchr11:75967408..75969952hg19UCSC Ensembl
Outerchr11:75967308..75970052hg19UCSC Ensembl
Cytoband11q13.5
Allele length
AssemblyAllele length
hg382645
hg192645
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv14214081
SamplesNA19225
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3626866
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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