A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3114292



Internal ID21297558
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:139900930..139907007hg38UCSC Ensembl
Innerchr6:140222067..140228144hg19UCSC Ensembl
Cytoband6q24.1
Allele length
AssemblyAllele length
hg386078
hg196078
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14087557
Samplessample181
Known Genes
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nsv3114292
Frequency
Sample Size467
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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