A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv590924



Internal ID16378333
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:89326283..89368137hg38UCSC Ensembl
Innerchr3:89375433..89417287hg19UCSC Ensembl
Innerchr3:89458123..89499977hg18UCSC Ensembl
Cytoband3p11.1
Allele length
AssemblyAllele length
hg3841855
hg1941855
hg1841855
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv8428n54
Supporting Variantsnssv967564, nssv967565
Samples
Known GenesEPHA3
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv590924
Frequency
Sample Size17421
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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