A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv5261n54



Internal ID22773156
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:84004904..84047164hg38UCSC Ensembl
chr16:84038509..84080769hg19UCSC Ensembl
chr16:82596010..82638270hg18UCSC Ensembl
Cytoband16q23.3
Allele length
AssemblyAllele length
hg3842261
hg1942261
hg1842261
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv573420, nsv573419
Samples
Known GenesSLC38A8
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)dgv5261n54
Frequency
Sample Size17421
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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