A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv566242



Internal ID16353651
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr14:105474277..105475240hg38UCSC Ensembl
Innerchr14:105940614..105941577hg19UCSC Ensembl
Innerchr14:105011659..105012622hg18UCSC Ensembl
Cytoband14q32.33
Allele length
AssemblyAllele length
hg38964
hg19964
hg18964
Variant TypeCNV gain+loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv3992n54
Supporting Variantsnssv834895, nssv834893, nssv834892, nssv834894, nssv834891
Samples
Known GenesCRIP2
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv566242
Frequency
Sample Size17421
Observed Gain2
Observed Loss3
Observed Complex0
Frequencyn/a


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