A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv5297n54



Internal ID20138721
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:88533592..88534620hg38UCSC Ensembl
chr16:88600000..88601028hg19UCSC Ensembl
chr16:87127501..87128529hg18UCSC Ensembl
Cytoband16q24.2
Allele length
AssemblyAllele length
hg381029
hg191029
hg181029
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv573604, nsv573601, nsv573603, nsv573598, nsv573602, nsv573599, nsv573600
Samples
Known GenesZFPM1
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)dgv5297n54
Frequency
Sample Size17421
Observed Gain0
Observed Loss12
Observed Complex0
Frequencyn/a


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