A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv569609



Internal ID16010332
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:60417705..60502450hg38UCSC Ensembl
Innerchr15:60709904..60794649hg19UCSC Ensembl
Innerchr15:58497196..58581941hg18UCSC Ensembl
Cytoband15q22.2
Allele length
AssemblyAllele length
hg3884746
hg1984746
hg1884746
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv843585
Samples
Known GenesNARG2, RORA
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv569609
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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