A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv4709n54



Internal ID20138133
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:90871209..90873320hg38UCSC Ensembl
chr15:91414439..91416550hg19UCSC Ensembl
chr15:89215443..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 Variants
Supporting Variantsnsv570429, nsv570422, nsv570416, nsv570404, nsv570410
Samples
Known GenesFURIN
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)dgv4709n54
Frequency
Sample Size17421
Observed Gain9
Observed Loss0
Observed Complex0
Frequencyn/a


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