A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1126037



Internal ID15979223
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:1311310..1662585hg38UCSC Ensembl
Innerchr9:1311310..1662585hg19UCSC Ensembl
Innerchr9:1301310..1652585hg18UCSC Ensembl
Cytoband9p24.3
Allele length
AssemblyAllele length
hg38351276
hg19351276
hg18351276
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv613052
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)nssv1126037
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