A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv552661



Internal ID15993384
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:133428733..133566995hg38UCSC Ensembl
Innerchr10:135242237..135380499hg19UCSC Ensembl
Innerchr10:135092227..135230489hg18UCSC Ensembl
Cytoband10q26.3
Allele length
AssemblyAllele length
hg38138263
hg19138263
hg18138263
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv1487n54
Supporting Variantsnssv762706, nssv762705
Samples
Known GenesCYP2E1, SCART1, SPRNP1, SYCE1
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv552661
Frequency
Sample Size17421
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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