A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv570400



Internal ID16011123
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:90871209..90872176hg38UCSC Ensembl
Innerchr15:91414439..91415406hg19UCSC Ensembl
Innerchr15:89215443..89216410hg18UCSC Ensembl
Cytoband15q26.1
Allele length
AssemblyAllele length
hg38968
hg19968
hg18968
Variant TypeCNV gain+loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv4706n54
Supporting Variantsnssv848217, nssv848218, nssv848216, nssv848219, nssv848220
Samples
Known GenesFURIN
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv570400
Frequency
Sample Size17421
Observed Gain3
Observed Loss2
Observed Complex0
Frequencyn/a


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