A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv570403



Internal ID16011126
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:90871209..90872387hg38UCSC Ensembl
Innerchr15:91414439..91415617hg19UCSC Ensembl
Innerchr15:89215443..89216621hg18UCSC Ensembl
Cytoband15q26.1
Allele length
AssemblyAllele length
hg381179
hg191179
hg181179
Variant TypeCNV gain+loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv4708n54
Supporting Variantsnssv848247, nssv848253, nssv848252, nssv848246, nssv848241, nssv848235, nssv848243, nssv848233, nssv848236, nssv848242, nssv848237, nssv848250, nssv848249, nssv848244, nssv848239, nssv848238, nssv848251, nssv848234, nssv848248, nssv848240, nssv848232, nssv848245
Samples
Known GenesFURIN
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv570403
Frequency
Sample Size17421
Observed Gain21
Observed Loss1
Observed Complex0
Frequencyn/a


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