A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1156560



Internal ID22086961
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:98155315..98188499hg38UCSC Ensembl
Outerchr6:98152352..98192304hg38UCSC Ensembl
Innerchr6:98603191..98636375hg19UCSC Ensembl
Outerchr6:98600228..98640180hg19UCSC Ensembl
Cytoband6q16.1
Allele length
AssemblyAllele length
hg3839953
hg1939953
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv4022497
Samples
Known Genes
MethodSNP array
AnalysisDefault settings
Platform
Comments
ReferenceLou_et_al_2014
Pubmed ID25026903
Accession Number(s)nsv1156560
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