A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv552244



Internal ID16339653
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:122034390..122083008hg38UCSC Ensembl
Innerchr10:123793905..123842523hg19UCSC Ensembl
Innerchr10:123783895..123832513hg18UCSC Ensembl
Cytoband10q26.13
Allele length
AssemblyAllele length
hg3848619
hg1948619
hg1848619
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv1407n54
Supporting Variantsnssv760311
Samples
Known GenesTACC2
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv552244
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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