A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3684177



Internal ID18982458
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:17756097..17851395hg38UCSC Ensembl
Innerchr8:17613606..17708904hg19UCSC Ensembl
Innerchr8:17657886..17753184hg18UCSC Ensembl
Cytoband8p22
Allele length
AssemblyAllele length
hg3895299
hg1995299
hg1895299
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1024711
Supporting Variants
Samples
Known GenesMTUS1
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3684177
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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