A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv590900



Internal ID16378309
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:85127899..85215861hg38UCSC Ensembl
Innerchr3:85177049..85265011hg19UCSC Ensembl
Innerchr3:85259739..85347701hg18UCSC Ensembl
Cytoband3p12.1
Allele length
AssemblyAllele length
hg3887963
hg1987963
hg1887963
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv8422n54
Supporting Variantsnssv967542
Samples
Known GenesCADM2
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv590900
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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