A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv551236



Internal ID16338645
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:65120965..65175775hg38UCSC Ensembl
Innerchr10:66880723..66935533hg19UCSC Ensembl
Innerchr10:66550729..66605539hg18UCSC Ensembl
Cytoband10q21.3
Allele length
AssemblyAllele length
hg3854811
hg1954811
hg1854811
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv1213n54
Supporting Variantsnssv749364
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv551236
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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