A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1134680



Internal ID15987866
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:41625832..41701115hg38UCSC Ensembl
Innerchr9:46095101..46170384hg19UCSC Ensembl
Innerchr9:45985097..46060380hg18UCSC Ensembl
Cytoband9p11.2
Allele length
AssemblyAllele length
hg3875284
hg1975284
hg1875284
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv614501
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)nssv1134680
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