A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv569947



Internal ID16357356
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:72508512..72586431hg38UCSC Ensembl
Innerchr15:72800853..72878772hg19UCSC Ensembl
Innerchr15:70587907..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 Variantsdgv4618n54
Supporting Variantsnssv845209
Samples
Known GenesARIH1
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv569947
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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