A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv590276



Internal ID16030999
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:51358140..51431657hg38UCSC Ensembl
Innerchr3:51395571..51469107hg19UCSC Ensembl
Innerchr3:51370611..51444147hg18UCSC Ensembl
Cytoband3p21.2
Allele length
AssemblyAllele length
hg3873518
hg1973537
hg1873537
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv963057
Samples
Known GenesDOCK3, MANF, RBM15B, VPRBP
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv590276
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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