A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv848317



Internal ID15795587
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:90871582..90872285hg38UCSC Ensembl
Innerchr15:91414812..91415515hg19UCSC Ensembl
Innerchr15:89215816..89216519hg18UCSC Ensembl
Cytoband15q26.1
Allele length
AssemblyAllele length
hg38704
hg19704
hg18704
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv570424
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)nssv848317
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