A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1154561



Internal ID22085066
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:208572669..208591490hg38UCSC Ensembl
Outerchr1:208567574..208596993hg38UCSC Ensembl
Innerchr1:208746014..208764835hg19UCSC Ensembl
Outerchr1:208740919..208770338hg19UCSC Ensembl
Cytoband1q32.2
Allele length
AssemblyAllele length
hg3829420
hg1929420
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv4007861
Samples
Known Genes
MethodSNP array
AnalysisDefault settings
Platform
Comments
ReferenceLou_et_al_2014
Pubmed ID25026903
Accession Number(s)nsv1154561
Frequency
Sample Size131
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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