A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv570418



Internal ID16011141
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:90871440..90872233hg38UCSC Ensembl
Innerchr15:91414670..91415463hg19UCSC Ensembl
Innerchr15:89215674..89216467hg18UCSC Ensembl
Cytoband15q26.1
Allele length
AssemblyAllele length
hg38794
hg19794
hg18794
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv4707n54
Supporting Variantsnssv848294, nssv848295, nssv848297, nssv848296
Samples
Known GenesFURIN
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv570418
Frequency
Sample Size17421
Observed Gain4
Observed Loss0
Observed Complex0
Frequencyn/a


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