A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3111301



Internal ID21294567
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr2:65923272..65934405hg38UCSC Ensembl
Innerchr2:66150406..66161539hg19UCSC Ensembl
Cytoband2p14
Allele length
AssemblyAllele length
hg3811134
hg1911134
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14104577
Samplessample130
Known Genes
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nsv3111301
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