A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1128531



Internal ID15981717
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:10753219..11280652hg38UCSC Ensembl
Innerchr9:10753219..11280652hg19UCSC Ensembl
Innerchr9:10743219..11270652hg18UCSC Ensembl
Cytoband9p23
Allele length
AssemblyAllele length
hg38527434
hg19527434
hg18527434
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv613407
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)nssv1128531
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