A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1155521



Internal ID22086026
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr18:61253545..61263000hg38UCSC Ensembl
Outerchr18:61250917..61271722hg38UCSC Ensembl
Innerchr18:58920778..58930233hg19UCSC Ensembl
Outerchr18:58918150..58938955hg19UCSC Ensembl
Cytoband18q21.32
Allele length
AssemblyAllele length
hg3820806
hg1920806
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv4011961
Samples
Known Genes
MethodSNP array
AnalysisDefault settings
Platform
Comments
ReferenceLou_et_al_2014
Pubmed ID25026903
Accession Number(s)nsv1155521
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