A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv9476n54



Internal ID20142900
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:356266..359196hg38UCSC Ensembl
chr5:356381..359311hg19UCSC Ensembl
chr5:409381..412311hg18UCSC Ensembl
Cytoband5p15.33
Allele length
AssemblyAllele length
hg382931
hg192931
hg182931
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv596615, nsv596617, nsv596619
Samples
Known GenesAHRR
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)dgv9476n54
Frequency
Sample Size17421
Observed Gain0
Observed Loss7
Observed Complex0
Frequencyn/a


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