A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv551286



Internal ID16338695
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:65550888..66450664hg38UCSC Ensembl
Innerchr10:67310646..68210422hg19UCSC Ensembl
Innerchr10:66980652..67880428hg18UCSC Ensembl
Cytoband10q21.3
Allele length
AssemblyAllele length
hg38899777
hg19899777
hg18899777
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv749774
Samples
Known GenesCTNNA3
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv551286
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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