A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1054621



Internal ID19143840
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:133451264..133534223hg38UCSC Ensembl
Innerchr10:135264768..135347727hg19UCSC Ensembl
Innerchr10:135114758..135197717hg18UCSC Ensembl
Cytoband10q26.3
Allele length
AssemblyAllele length
hg3882960
hg1982960
hg1882960
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv1005n100
Supporting Variantsnssv3522732
Samples
Known GenesCYP2E1, SCART1
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1054621
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