A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1156360



Internal ID22086761
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr5:91328710..91335567hg38UCSC Ensembl
Outerchr5:91325252..91342151hg38UCSC Ensembl
Innerchr5:90624527..90631384hg19UCSC Ensembl
Outerchr5:90621069..90637968hg19UCSC Ensembl
Cytoband5q14.3
Allele length
AssemblyAllele length
hg3816900
hg1916900
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv4018936, nssv4018935
Samples
Known Genes
MethodSNP array
AnalysisDefault settings
Platform
Comments
ReferenceLou_et_al_2014
Pubmed ID25026903
Accession Number(s)nsv1156360
Frequency
Sample Size131
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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