A curated catalogue of human genomic structural variation




Variant Details

Variant: essv14207093



Internal ID3459855
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:70055959..70057102hg38UCSC Ensembl
Innerchr11:70055961..70057101hg38UCSC Ensembl
Outerchr11:70055958..70057104hg38UCSC Ensembl
chr11:69902065..69903208hg19UCSC Ensembl
Innerchr11:69902067..69903207hg19UCSC Ensembl
Outerchr11:69902064..69903210hg19UCSC Ensembl
Cytoband11q13.3
Allele length
AssemblyAllele length
hg381144
hg191144
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3626759
Supporting Variants
SamplesHG03082
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv14207093
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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