A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv5298n54



Internal ID20138722
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:88533696..88547771hg38UCSC Ensembl
chr16:88600104..88614179hg19UCSC Ensembl
chr16:87127605..87141680hg18UCSC Ensembl
Cytoband16q24.2
Allele length
AssemblyAllele length
hg3814076
hg1914076
hg1814076
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv573606, nsv573605
Samples
Known GenesZFPM1
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)dgv5298n54
Frequency
Sample Size17421
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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