A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv9478n54



Internal ID20142902
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:391653..392411hg38UCSC Ensembl
chr5:391768..392526hg19UCSC Ensembl
chr5:444768..445526hg18UCSC Ensembl
Cytoband5p15.33
Allele length
AssemblyAllele length
hg38759
hg19759
hg18759
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv596625, nsv596624
Samples
Known GenesAHRR
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)dgv9478n54
Frequency
Sample Size17421
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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