A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv615120



Internal ID16055843
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:105773049..105775421hg38UCSC Ensembl
Innerchr9:108535330..108537702hg19UCSC Ensembl
Innerchr9:107575151..107577523hg18UCSC Ensembl
Cytoband9q31.2
Allele length
AssemblyAllele length
hg382373
hg192373
hg182373
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv12837n54
Supporting Variantsnssv1141001
Samples
Known GenesTMEM38B
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv615120
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