A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1022792



Internal ID18765326
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:18981254..19001299hg38UCSC Ensembl
Innerchr8:18838764..18858809hg19UCSC Ensembl
Innerchr8:18883044..18903089hg18UCSC Ensembl
Cytoband8p22
Allele length
AssemblyAllele length
hg3820046
hg1920046
hg1820046
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv7126n100
Supporting Variantsnssv3684205, nssv3684206, nssv3684204
Samples
Known GenesPSD3
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1022792
Frequency
Sample Size29084
Observed Gain0
Observed Loss3
Observed Complex0
Frequencyn/a


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