A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14098088



Internal ID21291012
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr17:21040786..21045047hg38UCSC Ensembl
Innerchr17:20944099..20948360hg19UCSC Ensembl
Cytoband17p11.2
Allele length
AssemblyAllele length
hg384262
hg194262
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3112972
Supporting Variants
Samplessample69
Known GenesUSP22
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nssv14098088
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