A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv590984



Internal ID16378393
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:90289369..90444732hg38UCSC Ensembl
Innerchr3:90338519..90493882hg19UCSC Ensembl
Innerchr3:90421209..90576572hg18UCSC Ensembl
Cytoband3p11.1
Allele length
AssemblyAllele length
hg38155364
hg19155364
hg18155364
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv8441n54
Supporting Variantsnssv967769
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv590984
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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