A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3113078



Internal ID21296344
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr17:32137342..32143338hg38UCSC Ensembl
Innerchr17:30464361..30470357hg19UCSC Ensembl
Cytoband17q11.2
Allele length
AssemblyAllele length
hg385997
hg195997
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14098908, nssv14097805
Samplessample152, sample295
Known GenesRHOT1
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nsv3113078
Frequency
Sample Size467
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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