A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv570407



Internal ID16011130
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:90871260..90872285hg38UCSC Ensembl
Innerchr15:91414490..91415515hg19UCSC Ensembl
Innerchr15:89215494..89216519hg18UCSC Ensembl
Cytoband15q26.1
Allele length
AssemblyAllele length
hg381026
hg191026
hg181026
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv4707n54
Supporting Variantsnssv848260, nssv848261
Samples
Known GenesFURIN
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv570407
Frequency
Sample Size17421
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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