A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3684200



Internal ID18635795
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:18977297..19001299hg38UCSC Ensembl
Innerchr8:18834807..18858809hg19UCSC Ensembl
Innerchr8:18879087..18903089hg18UCSC Ensembl
Cytoband8p22
Allele length
AssemblyAllele length
hg3824003
hg1924003
hg1824003
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1023156
Supporting Variants
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)nssv3684200
Frequency
Sample Size29084
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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