A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv614303



Internal ID16401712
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:67330186..67419720hg38UCSC Ensembl
Innerchr9:40064995..40158577hg19UCSC Ensembl
Innerchr9:40054995..40148577hg18UCSC Ensembl
Cytoband9p13.1
Allele length
AssemblyAllele length
hg3889535
hg1993583
hg1893583
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv12695n54
Supporting Variantsnssv1134119, nssv1134120
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv614303
Frequency
Sample Size17421
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer