A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv598942



Internal ID16386351
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr5:93222263..93275952hg38UCSC Ensembl
Innerchr5:92557969..92611658hg19UCSC Ensembl
Innerchr5:92583725..92637414hg18UCSC Ensembl
Cytoband5q15
Allele length
AssemblyAllele length
hg3853690
hg1953690
hg1853690
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1153050
SamplesHGDP00143
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv598942
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