A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv570402



Internal ID16011125
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:90871209..90872336hg38UCSC Ensembl
Innerchr15:91414439..91415566hg19UCSC Ensembl
Innerchr15:89215443..89216570hg18UCSC Ensembl
Cytoband15q26.1
Allele length
AssemblyAllele length
hg381128
hg191128
hg181128
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv4707n54
Supporting Variantsnssv848229, nssv848227, nssv848231, nssv848224, nssv848230, nssv848226, nssv848225, nssv848228
Samples
Known GenesFURIN
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv570402
Frequency
Sample Size17421
Observed Gain8
Observed Loss0
Observed Complex0
Frequencyn/a


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