A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3114069



Internal ID21297335
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr17:19866890..19868956hg38UCSC Ensembl
Innerchr17:19770203..19772269hg19UCSC Ensembl
Cytoband17p11.2
Allele length
AssemblyAllele length
hg382067
hg192067
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv484n145
Supporting Variantsnssv14097995, nssv14097789
Samplessample289, sample33
Known GenesULK2
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nsv3114069
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