A curated catalogue of human genomic structural variation




Variant Details

Variant: essv15416406



Internal ID967988
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:22418547..22435682hg38UCSC Ensembl
chr16:22429868..22447003hg19UCSC Ensembl
Cytoband16p12.2
Allele length
AssemblyAllele length
hg3817136
hg1917136
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3638206
Supporting Variants
SamplesHG00596
Known GenesRRN3P3
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv15416406
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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