A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv569798



Internal ID16357207
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:67122087..67142010hg38UCSC Ensembl
Innerchr15:67414425..67434348hg19UCSC Ensembl
Innerchr15:65201479..65221402hg18UCSC Ensembl
Cytoband15q22.33
Allele length
AssemblyAllele length
hg3819924
hg1919924
hg1819924
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1149235
SamplesNINDS_197
Known GenesSMAD3
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv569798
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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