A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv590899



Internal ID16378308
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:85114017..85342522hg38UCSC Ensembl
Innerchr3:85163167..85391672hg19UCSC Ensembl
Innerchr3:85245857..85474362hg18UCSC Ensembl
Cytoband3p12.1
Allele length
AssemblyAllele length
hg38228506
hg19228506
hg18228506
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv967541
Samples
Known GenesCADM2
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv590899
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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