A curated catalogue of human genomic structural variation




Variant Details

Variant: essv8951525



Internal ID14427360
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:11650363..11650390hg38UCSC Ensembl
Innerchr11:11650367..11650386hg38UCSC Ensembl
Outerchr11:11650340..11650413hg38UCSC Ensembl
chr11:11671910..11671937hg19UCSC Ensembl
Innerchr11:11671914..11671933hg19UCSC Ensembl
Outerchr11:11671887..11671960hg19UCSC Ensembl
chr11:11628486..11628513hg18UCSC Ensembl
Innerchr11:11628509..11628490hg18UCSC Ensembl
Outerchr11:11628463..11628536hg18UCSC Ensembl
Cytoband11p15.3
Allele length
AssemblyAllele length
hg38286
hg19286
hg18286
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3440261
Supporting Variants
SamplesNA18912
Known Genes
MethodSequencing
Analysis
PlatformIllumina
Comments
Reference1000_Genomes_Consortium_Pilot_Project
Pubmed ID20981092
Accession Number(s)essv8951525
Frequency
Sample Size185
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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