A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv5156n54



Internal ID22773051
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:58614185..58619934hg38UCSC Ensembl
chr16:58648089..58653838hg19UCSC Ensembl
chr16:57205590..57211339hg18UCSC Ensembl
Cytoband16q21
Allele length
AssemblyAllele length
hg385750
hg195750
hg185750
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv572784, nsv572778, nsv572789
Samples
Known GenesCNOT1
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)dgv5156n54
Frequency
Sample Size17421
Observed Gain0
Observed Loss9
Observed Complex0
Frequencyn/a


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