A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv570430



Internal ID16011153
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:90871778..90871904hg38UCSC Ensembl
Innerchr15:91415008..91415134hg19UCSC Ensembl
Innerchr15:89216012..89216138hg18UCSC Ensembl
Cytoband15q26.1
Allele length
AssemblyAllele length
hg38127
hg19127
hg18127
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv848343
Samples
Known GenesFURIN
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv570430
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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