A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1130796



Internal ID15637296
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:20668316..20793446hg38UCSC Ensembl
Innerchr9:20668315..20793445hg19UCSC Ensembl
Innerchr9:20658315..20783445hg18UCSC Ensembl
Cytoband9p21.3
Allele length
AssemblyAllele length
hg38125131
hg19125131
hg18125131
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv613747
Supporting Variants
Samples
Known GenesFOCAD, MIR491
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv1130796
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