A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv568750



Internal ID16009473
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:30606930..30796240hg38UCSC Ensembl
Innerchr15:30899133..31088443hg19UCSC Ensembl
Innerchr15:28686425..28875735hg18UCSC Ensembl
Cytoband15q13.2
Allele length
AssemblyAllele length
hg38189311
hg19189311
hg18189311
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv4425n54
Supporting Variantsnssv839479, nssv839480
Samples
Known GenesARHGAP11B, GOLGA8H, LOC100288637
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv568750
Frequency
Sample Size17421
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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