A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3627272



Internal ID7014102
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:92291521..92294805hg38UCSC Ensembl
Innerchr11:92291522..92294805hg38UCSC Ensembl
Outerchr11:92291521..92294806hg38UCSC Ensembl
chr11:92024687..92027971hg19UCSC Ensembl
Innerchr11:92024688..92027971hg19UCSC Ensembl
Outerchr11:92024687..92027972hg19UCSC Ensembl
Cytoband11q14.3
Allele length
AssemblyAllele length
hg383285
hg193285
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv14234129, essv14234126, essv14234133, essv14234130, essv14234128, essv14234131, essv14234127, essv14234132
SamplesHG00318, HG00251, NA20342, HG01122, HG00250, HG00310, HG01775, HG00362
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3627272
Frequency
Sample Size2504
Observed Gain0
Observed Loss8
Observed Complex0
Frequencyn/a


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