A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv5320n54



Internal ID20138744
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:89114475..89197443hg38UCSC Ensembl
chr16:89180883..89263851hg19UCSC Ensembl
chr16:87708384..87791352hg18UCSC Ensembl
Cytoband16q24.3
Allele length
AssemblyAllele length
hg3882969
hg1982969
hg1882969
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv573726, nsv573725
Samples
Known GenesACSF3, CDH15, LINC00304, LOC400558, SLC22A31
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)dgv5320n54
Frequency
Sample Size17421
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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