A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv596636



Internal ID16384045
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr5:467509..472299hg38UCSC Ensembl
Innerchr5:467624..472414hg19UCSC Ensembl
Innerchr5:520624..525414hg18UCSC Ensembl
Cytoband5p15.33
Allele length
AssemblyAllele length
hg384791
hg194791
hg184791
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv9482n54
Supporting Variantsnssv1021150
Samples
Known GenesPP7080
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv596636
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