A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv570421



Internal ID16011144
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:90871440..90872387hg38UCSC Ensembl
Innerchr15:91414670..91415617hg19UCSC Ensembl
Innerchr15:89215674..89216621hg18UCSC Ensembl
Cytoband15q26.1
Allele length
AssemblyAllele length
hg38948
hg19948
hg18948
Variant TypeCNV gain+loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv4706n54
Supporting Variantsnssv848304, nssv848309, nssv848305, nssv848307, nssv848306, nssv848308
Samples
Known GenesFURIN
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv570421
Frequency
Sample Size17421
Observed Gain5
Observed Loss1
Observed Complex0
Frequencyn/a


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