A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv569066



Internal ID16009789
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:34438557..34546808hg38UCSC Ensembl
Innerchr15:34730758..34839009hg19UCSC Ensembl
Innerchr15:32518050..32626301hg18UCSC Ensembl
Cytoband15q14
Allele length
AssemblyAllele length
hg38108252
hg19108252
hg18108252
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv4476n54
Supporting Variantsnssv840242, nssv840239, nssv840240, nssv840245, nssv840238, nssv840246, nssv840241, nssv840247, nssv840243, nssv840248, nssv840244, nssv840249
Samples
Known GenesGOLGA8B, MIR1233-1, MIR1233-2
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv569066
Frequency
Sample Size17421
Observed Gain0
Observed Loss12
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer