A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3332666



Internal ID15179653
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:120875928..120876441hg38UCSC Ensembl
Innerchr11:120875927..120876442hg38UCSC Ensembl
Outerchr11:120875818..120876561hg38UCSC Ensembl
chr11:120746637..120747150hg19UCSC Ensembl
Innerchr11:120746636..120747151hg19UCSC Ensembl
Outerchr11:120746527..120747270hg19UCSC Ensembl
chr11:120251847..120252360hg18UCSC Ensembl
Innerchr11:120252361..120251846hg18UCSC Ensembl
Outerchr11:120251737..120252480hg18UCSC Ensembl
Cytoband11q23.3
Allele length
AssemblyAllele length
hg38514
hg19514
hg18514
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv8808547
SamplesNA12878
Known GenesGRIK4
MethodSequencing
Analysis
Platform454
Comments
Reference1000_Genomes_Consortium_Pilot_Project
Pubmed ID20981092
Accession Number(s)esv3332666
Frequency
Sample Size185
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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