A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv590993



Internal ID16378402
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:95040660..95122498hg38UCSC Ensembl
Innerchr3:94759504..94841342hg19UCSC Ensembl
Innerchr3:96242194..96324032hg18UCSC Ensembl
Cytoband3q11.2
Allele length
AssemblyAllele length
hg3881839
hg1981839
hg1881839
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv967788
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv590993
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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