A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv5295n54



Internal ID20138719
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:88533472..88534620hg38UCSC Ensembl
chr16:88599880..88601028hg19UCSC Ensembl
chr16:87127381..87128529hg18UCSC Ensembl
Cytoband16q24.2
Allele length
AssemblyAllele length
hg381149
hg191149
hg181149
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv573592, nsv573597, nsv573591
Samples
Known GenesZFPM1
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)dgv5295n54
Frequency
Sample Size17421
Observed Gain7
Observed Loss0
Observed Complex0
Frequencyn/a


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