A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv552657



Internal ID15993380
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:133412162..133620799hg38UCSC Ensembl
Innerchr10:135225666..135434303hg19UCSC Ensembl
Innerchr10:135075656..135284293hg18UCSC Ensembl
Cytoband10q26.3
Allele length
AssemblyAllele length
hg38208638
hg19208638
hg18208638
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv1486n54
Supporting Variantsnssv762700, nssv762698, nssv762699
Samples
Known GenesCYP2E1, MTG1, SCART1, SPRN, SPRNP1, SYCE1
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv552657
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