A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv570426



Internal ID16011149
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:90871582..90872387hg38UCSC Ensembl
Innerchr15:91414812..91415617hg19UCSC Ensembl
Innerchr15:89215816..89216621hg18UCSC Ensembl
Cytoband15q26.1
Allele length
AssemblyAllele length
hg38806
hg19806
hg18806
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv848332, nssv848334, nssv848329, nssv848330, nssv848333, nssv848331
Samples
Known GenesFURIN
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv570426
Frequency
Sample Size17421
Observed Gain6
Observed Loss0
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer