A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv848316



Internal ID15795586
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:90871582..90872233hg38UCSC Ensembl
Innerchr15:91414812..91415463hg19UCSC Ensembl
Innerchr15:89215816..89216467hg18UCSC Ensembl
Cytoband15q26.1
Allele length
AssemblyAllele length
hg38652
hg19652
hg18652
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv570423
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)nssv848316
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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