A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv570427



Internal ID16011150
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:90871634..90872336hg38UCSC Ensembl
Innerchr15:91414864..91415566hg19UCSC Ensembl
Innerchr15:89215868..89216570hg18UCSC Ensembl
Cytoband15q26.1
Allele length
AssemblyAllele length
hg38703
hg19703
hg18703
Variant TypeCNV gain+loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv4710n54
Supporting Variantsnssv848339, nssv848338, nssv848335, nssv848340, nssv848336, nssv848337
Samples
Known GenesFURIN
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv570427
Frequency
Sample Size17421
Observed Gain5
Observed Loss1
Observed Complex0
Frequencyn/a


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