A curated catalogue of human genomic structural variation




Variant Details

Variant: essv14241837



Internal ID3129374
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:94669085..94672957hg38UCSC Ensembl
Innerchr11:94669117..94672926hg38UCSC Ensembl
Outerchr11:94669054..94672989hg38UCSC Ensembl
chr11:94402251..94406123hg19UCSC Ensembl
Innerchr11:94402283..94406092hg19UCSC Ensembl
Outerchr11:94402220..94406155hg19UCSC Ensembl
Cytoband11q21
Allele length
AssemblyAllele length
hg383873
hg193873
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3627322
Supporting Variants
SamplesHG02759
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv14241837
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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