A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1156040



Internal ID22086545
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:163734181..163866257hg38UCSC Ensembl
Outerchr3:163728146..163869563hg38UCSC Ensembl
Innerchr3:163451969..163584045hg19UCSC Ensembl
Outerchr3:163445934..163587351hg19UCSC Ensembl
Cytoband3q26.1
Allele length
AssemblyAllele length
hg38141418
hg19141418
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv4016093
Samples
Known Genes
MethodSNP array
AnalysisDefault settings
Platform
Comments
ReferenceLou_et_al_2014
Pubmed ID25026903
Accession Number(s)nsv1156040
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