A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv570399



Internal ID16011122
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:90871209..90872118hg38UCSC Ensembl
Innerchr15:91414439..91415348hg19UCSC Ensembl
Innerchr15:89215443..89216352hg18UCSC Ensembl
Cytoband15q26.1
Allele length
AssemblyAllele length
hg38910
hg19910
hg18910
Variant TypeCNV gain+loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv4706n54
Supporting Variantsnssv848212, nssv848215, nssv848213, nssv848214
Samples
Known GenesFURIN
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv570399
Frequency
Sample Size17421
Observed Gain2
Observed Loss2
Observed Complex0
Frequencyn/a


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