A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14097612



Internal ID21273904
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr17:28811646..28813263hg38UCSC Ensembl
Innerchr17:27138664..27140281hg19UCSC Ensembl
Cytoband17q11.2
Allele length
AssemblyAllele length
hg381618
hg191618
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3114154
Supporting Variants
Samplessample198
Known GenesFAM222B
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nssv14097612
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