A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv570434



Internal ID16011157
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:90871778..90875361hg38UCSC Ensembl
Innerchr15:91415008..91418591hg19UCSC Ensembl
Innerchr15:89216012..89219595hg18UCSC Ensembl
Cytoband15q26.1
Allele length
AssemblyAllele length
hg383584
hg193584
hg183584
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv848356
Samples
Known GenesFURIN
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv570434
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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