A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv613917



Internal ID16401326
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:25628821..25661722hg38UCSC Ensembl
Innerchr9:25628819..25661720hg19UCSC Ensembl
Innerchr9:25618819..25651720hg18UCSC Ensembl
Cytoband9p21.2
Allele length
AssemblyAllele length
hg3832902
hg1932902
hg1832902
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv12615n54
Supporting Variantsnssv1132049
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv613917
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