A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv598884



Internal ID16386293
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr5:86950206..86975107hg38UCSC Ensembl
Innerchr5:86246023..86270924hg19UCSC Ensembl
Innerchr5:86281779..86306680hg18UCSC Ensembl
Cytoband5q14.3
Allele length
AssemblyAllele length
hg3824902
hg1924902
hg1824902
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1036119
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv598884
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