A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv568927



Internal ID16009650
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:34379904..34470157hg38UCSC Ensembl
Innerchr15:34672105..34762358hg19UCSC Ensembl
Innerchr15:32459397..32549650hg18UCSC Ensembl
Cytoband15q14
Allele length
AssemblyAllele length
hg3890254
hg1990254
hg1890254
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv4458n54
Supporting Variantsnssv839803
Samples
Known GenesGOLGA8A, MIR1233-1, MIR1233-2
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv568927
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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