A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1155990



Internal ID22086495
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:77778305..77792721hg38UCSC Ensembl
Outerchr3:77775868..77801580hg38UCSC Ensembl
Innerchr3:77827456..77841872hg19UCSC Ensembl
Outerchr3:77825019..77850731hg19UCSC Ensembl
Cytoband3p12.3
Allele length
AssemblyAllele length
hg3825713
hg1925713
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv4017626
Samples
Known Genes
MethodSNP array
AnalysisDefault settings
Platform
Comments
ReferenceLou_et_al_2014
Pubmed ID25026903
Accession Number(s)nsv1155990
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