A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv552249



Internal ID16339658
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:122146687..122166795hg38UCSC Ensembl
Innerchr10:123906202..123926310hg19UCSC Ensembl
Innerchr10:123896192..123916300hg18UCSC Ensembl
Cytoband10q26.13
Allele length
AssemblyAllele length
hg3820109
hg1920109
hg1820109
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv1408n54
Supporting Variantsnssv760316, nssv760317, nssv760315
Samples
Known GenesTACC2
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv552249
Frequency
Sample Size17421
Observed Gain0
Observed Loss3
Observed Complex0
Frequencyn/a


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