A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1155973



Internal ID22086478
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:74434836..74535454hg38UCSC Ensembl
Outerchr3:74432753..74541861hg38UCSC Ensembl
Innerchr3:74483987..74584605hg19UCSC Ensembl
Outerchr3:74481904..74591012hg19UCSC Ensembl
Cytoband3p12.3
Allele length
AssemblyAllele length
hg38109109
hg19109109
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv4016406
Samples
Known GenesCNTN3
MethodSNP array
AnalysisDefault settings
Platform
Comments
ReferenceLou_et_al_2014
Pubmed ID25026903
Accession Number(s)nsv1155973
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