A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv590908



Internal ID16378317
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:85604283..85638402hg38UCSC Ensembl
Innerchr3:85653433..85687552hg19UCSC Ensembl
Innerchr3:85736123..85770242hg18UCSC Ensembl
Cytoband3p12.1
Allele length
AssemblyAllele length
hg3834120
hg1934120
hg1834120
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv8424n54
Supporting Variantsnssv967550, nssv967551
Samples
Known GenesCADM2
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv590908
Frequency
Sample Size17421
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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