A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv564911



Internal ID16352320
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr14:65138010..65141099hg38UCSC Ensembl
Innerchr14:65604728..65607817hg19UCSC Ensembl
Innerchr14:64674481..64677570hg18UCSC Ensembl
Cytoband14q23.3
Allele length
AssemblyAllele length
hg383090
hg193090
hg183090
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv3724n54
Supporting Variantsnssv828243
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv564911
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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