A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1141290



Internal ID15994476
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:117462732..117502976hg38UCSC Ensembl
Innerchr9:120225010..120265254hg19UCSC Ensembl
Innerchr9:119264831..119305075hg18UCSC Ensembl
Cytoband9q33.1
Allele length
AssemblyAllele length
hg3840245
hg1940245
hg1840245
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv615263
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)nssv1141290
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