A curated catalogue of human genomic structural variation




Variant Details

Variant: essv14026144



Internal ID3233402
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:10106844..10192351hg38UCSC Ensembl
Innerchr11:10106875..10192320hg38UCSC Ensembl
Outerchr11:10106813..10192382hg38UCSC Ensembl
chr11:10128391..10213898hg19UCSC Ensembl
Innerchr11:10128422..10213867hg19UCSC Ensembl
Outerchr11:10128360..10213929hg19UCSC Ensembl
Cytoband11p15.4
Allele length
AssemblyAllele length
hg3885508
hg1985508
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3625347
Supporting Variants
SamplesHG02851
Known GenesSBF2
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv14026144
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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