A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv590922



Internal ID16378331
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:89265712..89367914hg38UCSC Ensembl
Innerchr3:89314862..89417064hg19UCSC Ensembl
Innerchr3:89397552..89499754hg18UCSC Ensembl
Cytoband3p11.1
Allele length
AssemblyAllele length
hg38102203
hg19102203
hg18102203
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv8427n54
Supporting Variantsnssv967562
Samples
Known GenesEPHA3
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv590922
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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