A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3627188



Internal ID7014018
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:90130184..90148445hg38UCSC Ensembl
Innerchr11:90130184..90148445hg38UCSC Ensembl
Outerchr11:90129684..90148945hg38UCSC Ensembl
chr11:89863352..89881613hg19UCSC Ensembl
Innerchr11:89863352..89881613hg19UCSC Ensembl
Outerchr11:89862852..89882113hg19UCSC Ensembl
Cytoband11q14.3
Allele length
AssemblyAllele length
hg3818262
hg1918262
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv14230906, essv14230905
SamplesHG02470, NA18631
Known GenesNAALAD2
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3627188
Frequency
Sample Size2504
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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