A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv967547



Internal ID16261503
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:85389414..85747943hg38UCSC Ensembl
Innerchr3:85438564..85797093hg19UCSC Ensembl
Innerchr3:85521254..85879783hg18UCSC Ensembl
Cytoband3p12.1
Allele length
AssemblyAllele length
hg38358530
hg19358530
hg18358530
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv590905
Supporting Variants
Samples
Known GenesCADM2
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv967547
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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