A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv552251



Internal ID16339660
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:122457266..122457796hg38UCSC Ensembl
Innerchr10:124216782..124217312hg19UCSC Ensembl
Innerchr10:124206772..124207302hg18UCSC Ensembl
Cytoband10q26.13
Allele length
AssemblyAllele length
hg38531
hg19531
hg18531
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv1409n54
Supporting Variantsnssv760319
Samples
Known GenesARMS2
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv552251
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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