A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv590898



Internal ID16378307
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:85109582..85194627hg38UCSC Ensembl
Innerchr3:85158733..85243777hg19UCSC Ensembl
Innerchr3:85241423..85326467hg18UCSC Ensembl
Cytoband3p12.1
Allele length
AssemblyAllele length
hg3885046
hg1985045
hg1885045
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv8422n54
Supporting Variantsnssv967540
Samples
Known GenesCADM2
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv590898
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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