A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv848265



Internal ID15795535
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:90871260..90872387hg38UCSC Ensembl
Innerchr15:91414490..91415617hg19UCSC Ensembl
Innerchr15:89215494..89216621hg18UCSC Ensembl
Cytoband15q26.1
Allele length
AssemblyAllele length
hg381128
hg191128
hg181128
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv570409
Supporting Variants
Samples
Known GenesFURIN
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv848265
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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