A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv570393



Internal ID16011116
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:90306286..90455896hg38UCSC Ensembl
Innerchr15:90849518..90999128hg19UCSC Ensembl
Innerchr15:88650522..88800132hg18UCSC Ensembl
Cytoband15q26.1
Allele length
AssemblyAllele length
hg38149611
hg19149611
hg18149611
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv4705n54
Supporting Variantsnssv848205, nssv848206
Samples
Known GenesGABARAPL3, IQGAP1, ZNF774
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv570393
Frequency
Sample Size17421
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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