A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv4618n54



Internal ID22772513
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:72508512..72586431hg38UCSC Ensembl
chr15:72800853..72878772hg19UCSC Ensembl
chr15:70587907..70665826hg18UCSC Ensembl
Cytoband15q24.1
Allele length
AssemblyAllele length
hg3877920
hg1977920
hg1877920
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv569947, nsv569948
Samples
Known GenesARIH1
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)dgv4618n54
Frequency
Sample Size17421
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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