A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv4706n54



Internal ID20138130
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+loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv570399, nsv570419, nsv570400, nsv570420, nsv570421, nsv570411, nsv570417
Samples
Known GenesFURIN
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)dgv4706n54
Frequency
Sample Size17421
Observed Gain24
Observed Loss12
Observed Complex0
Frequencyn/a


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