A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv615465



Internal ID16402874
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:129453264..129466427hg38UCSC Ensembl
Innerchr9:132215543..132228706hg19UCSC Ensembl
Innerchr9:131255364..131268527hg18UCSC Ensembl
Cytoband9q34.11
Allele length
AssemblyAllele length
hg3813164
hg1913164
hg1813164
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv12902n54
Supporting Variantsnssv1145030
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv615465
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