A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv5327n54



Internal ID22773222
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:89830015..89832059hg38UCSC Ensembl
chr16:89896423..89898467hg19UCSC Ensembl
chr16:88423924..88425968hg18UCSC Ensembl
Cytoband16q24.3
Allele length
AssemblyAllele length
hg382045
hg192045
hg182045
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv573767, nsv573777, nsv573763, nsv573783, nsv573764, nsv573759, nsv573757, nsv573762, nsv573779, nsv573771, nsv573756, nsv573772, nsv573773, nsv573755, nsv573784, nsv573782, nsv573766, nsv573778, nsv573769, nsv573758, nsv573774, nsv573768
Samples
Known GenesSPIRE2
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)dgv5327n54
Frequency
Sample Size17421
Observed Gain0
Observed Loss184
Observed Complex0
Frequencyn/a


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