A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv570404



Internal ID16011127
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:90871209..90873320hg38UCSC Ensembl
Innerchr15:91414439..91416550hg19UCSC Ensembl
Innerchr15:89215443..89217554hg18UCSC Ensembl
Cytoband15q26.1
Allele length
AssemblyAllele length
hg382112
hg192112
hg182112
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv4709n54
Supporting Variantsnssv848256, nssv848257, nssv848254, nssv848255
Samples
Known GenesFURIN
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv570404
Frequency
Sample Size17421
Observed Gain4
Observed Loss0
Observed Complex0
Frequencyn/a


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