A curated catalogue of human genomic structural variation




Variant Details

Variant: essv16151938



Internal ID842898
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:16579484..16692147hg38UCSC Ensembl
chr20:16560129..16672792hg19UCSC Ensembl
Cytoband20p12.1
Allele length
AssemblyAllele length
hg38112664
hg19112664
Variant TypeCNV gain
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3645406
Supporting Variants
SamplesHG00437
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv16151938
Frequency
Sample Size2504
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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