A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv762988



Internal ID15710258
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:133481130..133567238hg38UCSC Ensembl
Innerchr10:135294634..135380742hg19UCSC Ensembl
Innerchr10:135144624..135230732hg18UCSC Ensembl
Cytoband10q26.3
Allele length
AssemblyAllele length
hg3886109
hg1986109
hg1886109
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv552709
Supporting Variants
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)nssv762988
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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