A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv590925



Internal ID16378334
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:89330785..89368021hg38UCSC Ensembl
Innerchr3:89379935..89417171hg19UCSC Ensembl
Innerchr3:89462625..89499861hg18UCSC Ensembl
Cytoband3p11.1
Allele length
AssemblyAllele length
hg3837237
hg1937237
hg1837237
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv8428n54
Supporting Variantsnssv967567, nssv967566
Samples
Known GenesEPHA3
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv590925
Frequency
Sample Size17421
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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