A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3111069



Internal ID21294335
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:45069021..45160301hg38UCSC Ensembl
Innerchr6:45036758..45128038hg19UCSC Ensembl
Cytoband6p21.1
Allele length
AssemblyAllele length
hg3891281
hg1991281
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14082926
Samplessample316
Known GenesSUPT3H
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nsv3111069
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