A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1134076



Internal ID15987262
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:38889198..39059233hg38UCSC Ensembl
Innerchr9:38889195..39059230hg19UCSC Ensembl
Innerchr9:38879195..39049230hg18UCSC Ensembl
Cytoband9p13.1
Allele length
AssemblyAllele length
hg38170036
hg19170036
hg18170036
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv614281
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)nssv1134076
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