A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1017084



Internal ID19106301
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:17755337..17836735hg38UCSC Ensembl
Innerchr8:17612846..17694244hg19UCSC Ensembl
Innerchr8:17657126..17738524hg18UCSC Ensembl
Cytoband8p22
Allele length
AssemblyAllele length
hg3881399
hg1981399
hg1881399
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv7120n100
Supporting Variantsnssv3684175
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)nsv1017084
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