A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv590985



Internal ID16378394
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:90290567..90438204hg38UCSC Ensembl
Innerchr3:90339717..90487354hg19UCSC Ensembl
Innerchr3:90422407..90570044hg18UCSC Ensembl
Cytoband3p11.1
Allele length
AssemblyAllele length
hg38147638
hg19147638
hg18147638
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv8441n54
Supporting Variantsnssv967770
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv590985
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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