A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv568531



Internal ID16355940
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:24821213..24861936hg38UCSC Ensembl
Innerchr15:25066360..25107083hg19UCSC Ensembl
Innerchr15:22617453..22658176hg18UCSC Ensembl
Cytoband15q11.2
Allele length
AssemblyAllele length
hg3840724
hg1940724
hg1840724
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv4376n54
Supporting Variantsnssv838765, nssv838766
Samples
Known GenesSNRPN
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv568531
Frequency
Sample Size17421
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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