A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1144838



Internal ID15998024
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:129453159..129466284hg38UCSC Ensembl
Innerchr9:132215438..132228563hg19UCSC Ensembl
Innerchr9:131255259..131268384hg18UCSC Ensembl
Cytoband9q34.11
Allele length
AssemblyAllele length
hg3813126
hg1913126
hg1813126
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv615454
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv1144838
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