A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv615123



Internal ID16055846
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:105773926..105775093hg38UCSC Ensembl
Innerchr9:108536207..108537374hg19UCSC Ensembl
Innerchr9:107576028..107577195hg18UCSC Ensembl
Cytoband9q31.2
Allele length
AssemblyAllele length
hg381168
hg191168
hg181168
Variant TypeCNV gain+loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv12839n54
Supporting Variantsnssv1141005, nssv1141006
Samples
Known GenesTMEM38B
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv615123
Frequency
Sample Size17421
Observed Gain1
Observed Loss1
Observed Complex0
Frequencyn/a


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