A curated catalogue of human genomic structural variation




Variant Details

Variant: essv7822029



Internal ID13116596
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:103865629..103865630hg38UCSC Ensembl
Innerchr11:103865611..103865648hg38UCSC Ensembl
Outerchr11:103865610..103865649hg38UCSC Ensembl
chr11:103736357..103736358hg19UCSC Ensembl
Innerchr11:103736339..103736376hg19UCSC Ensembl
Outerchr11:103736338..103736377hg19UCSC Ensembl
chr11:103241567..103241568hg18UCSC Ensembl
Innerchr11:103241586..103241549hg18UCSC Ensembl
Outerchr11:103241548..103241587hg18UCSC Ensembl
Cytoband11q22.3
Allele length
AssemblyAllele length
hg38294
hg19294
hg18294
Variant TypeCNV mobile element insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3303430
Supporting Variants
SamplesNA11829
Known Genes
MethodSequencing
Analysis
PlatformRoche 454
Comments
Reference1000_Genomes_Consortium_Pilot_Project
Pubmed ID20981092
Accession Number(s)essv7822029
Frequency
Sample Size185
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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