A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv550286



Internal ID16337695
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:28369346..28375723hg38UCSC Ensembl
Innerchr10:28658275..28664652hg19UCSC Ensembl
Innerchr10:28698281..28704658hg18UCSC Ensembl
Cytoband10p11.23
Allele length
AssemblyAllele length
hg386378
hg196378
hg186378
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv1015n54
Supporting Variantsnssv745549
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv550286
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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