A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv570398



Internal ID16011121
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:90868426..90872336hg38UCSC Ensembl
Innerchr15:91411656..91415566hg19UCSC Ensembl
Innerchr15:89212660..89216570hg18UCSC Ensembl
Cytoband15q26.1
Allele length
AssemblyAllele length
hg383911
hg193911
hg183911
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv848211
Samples
Known GenesFURIN
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv570398
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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