A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3587376



Internal ID18538971
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr22:20208946..20248450hg38UCSC Ensembl
Innerchr22:20196469..20235973hg19UCSC Ensembl
Innerchr22:18576469..18615973hg18UCSC Ensembl
Cytoband22q11.21
Allele length
AssemblyAllele length
hg3839505
hg1939505
hg1839505
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1064701
Supporting Variants
Samples
Known GenesRTN4R
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3587376
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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