A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv596598



Internal ID16037321
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr5:83517..90084hg38UCSC Ensembl
Innerchr5:83632..90199hg19UCSC Ensembl
Innerchr5:136632..143199hg18UCSC Ensembl
Cytoband5p15.33
Allele length
AssemblyAllele length
hg386568
hg196568
hg186568
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1021038
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv596598
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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