A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv848259



Internal ID15795529
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:90871260..90872118hg38UCSC Ensembl
Innerchr15:91414490..91415348hg19UCSC Ensembl
Innerchr15:89215494..89216352hg18UCSC Ensembl
Cytoband15q26.1
Allele length
AssemblyAllele length
hg38859
hg19859
hg18859
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv570406
Supporting Variants
Samples
Known GenesFURIN
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv848259
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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