A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv592062



Internal ID16032785
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:151796802..151856498hg38UCSC Ensembl
Innerchr3:151514590..151574286hg19UCSC Ensembl
Innerchr3:152997280..153056976hg18UCSC Ensembl
Cytoband3q25.1
Allele length
AssemblyAllele length
hg3859697
hg1959697
hg1859697
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv8654n54
Supporting Variantsnssv976837
Samples
Known GenesAADAC, MIR548H2
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv592062
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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