A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv599410



Internal ID16386819
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr5:113799037..113844940hg38UCSC Ensembl
Innerchr5:113134734..113180637hg19UCSC Ensembl
Innerchr5:113162633..113208536hg18UCSC Ensembl
Cytoband5q22.3
Allele length
AssemblyAllele length
hg3845904
hg1945904
hg1845904
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv10013n54
Supporting Variantsnssv1040406
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv599410
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