A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv4707n54



Internal ID20138131
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:90871209..90872387hg38UCSC Ensembl
chr15:91414439..91415617hg19UCSC Ensembl
chr15:89215443..89216621hg18UCSC Ensembl
Cytoband15q26.1
Allele length
AssemblyAllele length
hg381179
hg191179
hg181179
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv570408, nsv570418, nsv570401, nsv570407, nsv570415, nsv570402, nsv570414, nsv570406, nsv570412, nsv570413
Samples
Known GenesFURIN
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)dgv4707n54
Frequency
Sample Size17421
Observed Gain28
Observed Loss0
Observed Complex0
Frequencyn/a


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