A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv566223



Internal ID16353632
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr14:105474172..105475033hg38UCSC Ensembl
Innerchr14:105940509..105941370hg19UCSC Ensembl
Innerchr14:105011554..105012415hg18UCSC Ensembl
Cytoband14q32.33
Allele length
AssemblyAllele length
hg38862
hg19862
hg18862
Variant TypeCNV gain+loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv3992n54
Supporting Variantsnssv834830, nssv834828, nssv834829
Samples
Known GenesCRIP2
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv566223
Frequency
Sample Size17421
Observed Gain2
Observed Loss1
Observed Complex0
Frequencyn/a


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