A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv552708



Internal ID15993431
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:133481130..133567061hg38UCSC Ensembl
Innerchr10:135294634..135380565hg19UCSC Ensembl
Innerchr10:135144624..135230555hg18UCSC Ensembl
Cytoband10q26.3
Allele length
AssemblyAllele length
hg3885932
hg1985932
hg1885932
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv1495n54
Supporting Variantsnssv762985, nssv762986, nssv762987
Samples
Known GenesCYP2E1, SPRNP1, SYCE1
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv552708
Frequency
Sample Size17421
Observed Gain3
Observed Loss0
Observed Complex0
Frequencyn/a


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