A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv592710



Internal ID16033433
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:187183211..187204160hg38UCSC Ensembl
Innerchr3:186900999..186921948hg19UCSC Ensembl
Innerchr3:188383693..188404642hg18UCSC Ensembl
Cytoband3q27.3
Allele length
AssemblyAllele length
hg3820950
hg1920950
hg1820950
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv982659
Samples
Known GenesRTP1
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv592710
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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