A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv4971n54



Internal ID20138395
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:28592568..28610911hg38UCSC Ensembl
chr16:28603889..28622232hg19UCSC Ensembl
chr16:28511390..28529733hg18UCSC Ensembl
Cytoband16p11.2
Allele length
AssemblyAllele length
hg3818344
hg1918344
hg1818344
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv571742, nsv571741
Samples
Known GenesSULT1A1, SULT1A2
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)dgv4971n54
Frequency
Sample Size17421
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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