A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv570435



Internal ID16011158
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:90871849..90873375hg38UCSC Ensembl
Innerchr15:91415079..91416605hg19UCSC Ensembl
Innerchr15:89216083..89217609hg18UCSC Ensembl
Cytoband15q26.1
Allele length
AssemblyAllele length
hg381527
hg191527
hg181527
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv4711n54
Supporting Variantsnssv848357
Samples
Known GenesFURIN
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv570435
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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