A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3638206



Internal ID7024992
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 State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv15416406, essv15416407
SamplesHG00596, HG01857
Known GenesRRN3P3
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3638206
Frequency
Sample Size2504
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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