A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv4711n54



Internal ID20138135
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:90871778..90873375hg38UCSC Ensembl
chr15:91415008..91416605hg19UCSC Ensembl
chr15:89216012..89217609hg18UCSC Ensembl
Cytoband15q26.1
Allele length
AssemblyAllele length
hg381598
hg191598
hg181598
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv570435, nsv570433
Samples
Known GenesFURIN
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)dgv4711n54
Frequency
Sample Size17421
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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