A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1131828



Internal ID15985014
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:24125020..24154730hg38UCSC Ensembl
Innerchr9:24125018..24154728hg19UCSC Ensembl
Innerchr9:24115018..24144728hg18UCSC Ensembl
Cytoband9p21.3
Allele length
AssemblyAllele length
hg3829711
hg1929711
hg1829711
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv613831
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)nssv1131828
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