A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv9487n54



Internal ID22777382
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:472193..473702hg38UCSC Ensembl
chr5:472308..473817hg19UCSC Ensembl
chr5:525308..526817hg18UCSC Ensembl
Cytoband5p15.33
Allele length
AssemblyAllele length
hg381510
hg191510
hg181510
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv596674, nsv596680, nsv596679
Samples
Known GenesPP7080, SLC9A3
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)dgv9487n54
Frequency
Sample Size17421
Observed Gain0
Observed Loss3
Observed Complex0
Frequencyn/a


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