A curated catalogue of human genomic structural variation




Variant Details

Variant: essv7741787



Internal ID13791329
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:11650363..11650364hg38UCSC Ensembl
Innerchr11:11650327..11650400hg38UCSC Ensembl
Outerchr11:11650326..11650401hg38UCSC Ensembl
chr11:11671910..11671911hg19UCSC Ensembl
Innerchr11:11671874..11671947hg19UCSC Ensembl
Outerchr11:11671873..11671948hg19UCSC Ensembl
chr11:11628486..11628487hg18UCSC Ensembl
Innerchr11:11628523..11628450hg18UCSC Ensembl
Outerchr11:11628449..11628524hg18UCSC Ensembl
Cytoband11p15.3
Allele length
AssemblyAllele length
hg38286
hg19286
hg18286
Variant TypeCNV mobile element insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3305258
Supporting Variants
SamplesNA18502
Known Genes
MethodSequencing
Analysis
PlatformIllumina
Comments
Reference1000_Genomes_Consortium_Pilot_Project
Pubmed ID20981092
Accession Number(s)essv7741787
Frequency
Sample Size185
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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