A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1156324



Internal ID22084800
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr5:25838958..25844609hg38UCSC Ensembl
Outerchr5:25829446..25851630hg38UCSC Ensembl
Innerchr5:25839067..25844718hg19UCSC Ensembl
Outerchr5:25829555..25851739hg19UCSC Ensembl
Cytoband5p14.1
Allele length
AssemblyAllele length
hg3822185
hg1922185
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv4020744
Samples
Known Genes
MethodSNP array
AnalysisDefault settings
Platform
Comments
ReferenceLou_et_al_2014
Pubmed ID25026903
Accession Number(s)nsv1156324
Frequency
Sample Size131
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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