A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv615200



Internal ID16402609
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:112953875..112983376hg38UCSC Ensembl
Innerchr9:115716155..115745656hg19UCSC Ensembl
Innerchr9:114755976..114785477hg18UCSC Ensembl
Cytoband9q32
Allele length
AssemblyAllele length
hg3829502
hg1929502
hg1829502
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv12852n54
Supporting Variantsnssv1176123
SamplesNINDS_232
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv615200
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