A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv552245



Internal ID16339654
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:122034390..122089950hg38UCSC Ensembl
Innerchr10:123793905..123849465hg19UCSC Ensembl
Innerchr10:123783895..123839455hg18UCSC Ensembl
Cytoband10q26.13
Allele length
AssemblyAllele length
hg3855561
hg1955561
hg1855561
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv1407n54
Supporting Variantsnssv760312
Samples
Known GenesTACC2
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv552245
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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