A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv596889



Internal ID16384298
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr5:1753191..1775485hg38UCSC Ensembl
Innerchr5:1753306..1775600hg19UCSC Ensembl
Innerchr5:1806306..1828600hg18UCSC Ensembl
Cytoband5p15.33
Allele length
AssemblyAllele length
hg3822295
hg1922295
hg1822295
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1022207
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv596889
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