A curated catalogue of human genomic structural variation




Variant Details

Variant: essv14280563



Internal ID2223410
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:109633726..109640549hg38UCSC Ensembl
Innerchr11:109633732..109640544hg38UCSC Ensembl
Outerchr11:109633721..109640555hg38UCSC Ensembl
chr11:109504452..109511275hg19UCSC Ensembl
Innerchr11:109504458..109511270hg19UCSC Ensembl
Outerchr11:109504447..109511281hg19UCSC Ensembl
Cytoband11q22.3
Allele length
AssemblyAllele length
hg386824
hg196824
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3627706
Supporting Variants
SamplesHG01997
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv14280563
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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