A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv16n54



Internal ID20133440
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:934429..935265hg38UCSC Ensembl
chr1:869809..870645hg19UCSC Ensembl
chr1:859672..860508hg18UCSC Ensembl
Cytoband1p36.33
Allele length
AssemblyAllele length
hg38837
hg19837
hg18837
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv544931, nsv544934
Samples
Known GenesSAMD11
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)dgv16n54
Frequency
Sample Size17421
Observed Gain0
Observed Loss9
Observed Complex0
Frequencyn/a


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