A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1141289



Internal ID15994475
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:117447749..117562075hg38UCSC Ensembl
Innerchr9:120210027..120324353hg19UCSC Ensembl
Innerchr9:119249848..119364174hg18UCSC Ensembl
Cytoband9q33.1
Allele length
AssemblyAllele length
hg38114327
hg19114327
hg18114327
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv615262
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)nssv1141289
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer