A curated catalogue of human genomic structural variation




Variant Details

Variant: essv14200105



Internal ID4201921
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:68299773..68301695hg38UCSC Ensembl
Innerchr11:68299804..68301665hg38UCSC Ensembl
Outerchr11:68299743..68301726hg38UCSC Ensembl
chr11:68067241..68069163hg19UCSC Ensembl
Innerchr11:68067272..68069133hg19UCSC Ensembl
Outerchr11:68067211..68069194hg19UCSC Ensembl
Cytoband11q13.2
Allele length
AssemblyAllele length
hg381923
hg191923
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3626736
Supporting Variants
SamplesHG00290
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv14200105
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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