A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv5308n54



Internal ID20138732
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:88572446..88573844hg38UCSC Ensembl
chr16:88638854..88640252hg19UCSC Ensembl
chr16:87166355..87167753hg18UCSC Ensembl
Cytoband16q24.2
Allele length
AssemblyAllele length
hg381399
hg191399
hg181399
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv573660, nsv573661, nsv573659
Samples
Known GenesZC3H18
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)dgv5308n54
Frequency
Sample Size17421
Observed Gain0
Observed Loss3
Observed Complex0
Frequencyn/a


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