A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv592410



Internal ID16379819
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:163139690..163258345hg38UCSC Ensembl
Innerchr3:162857478..162976133hg19UCSC Ensembl
Innerchr3:164340172..164458827hg18UCSC Ensembl
Cytoband3q26.1
Allele length
AssemblyAllele length
hg38118656
hg19118656
hg18118656
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv981066
Samples
Known GenesCT64
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv592410
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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