A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv5754n54



Internal ID20139178
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:67982311..67994016hg38UCSC Ensembl
chr17:65978427..65990132hg19UCSC Ensembl
chr17:63408889..63420594hg18UCSC Ensembl
Cytoband17q24.2
Allele length
AssemblyAllele length
hg3811706
hg1911706
hg1811706
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv575919, nsv575918
Samples
Known GenesBPTF, C17orf58
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)dgv5754n54
Frequency
Sample Size17421
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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