A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv570405



Internal ID16011128
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:90871209..90875361hg38UCSC Ensembl
Innerchr15:91414439..91418591hg19UCSC Ensembl
Innerchr15:89215443..89219595hg18UCSC Ensembl
Cytoband15q26.1
Allele length
AssemblyAllele length
hg384153
hg194153
hg184153
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv848258
Samples
Known GenesFURIN
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv570405
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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