A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv592048



Internal ID16032771
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:151792469..151875430hg38UCSC Ensembl
Innerchr3:151510257..151593218hg19UCSC Ensembl
Innerchr3:152992947..153075908hg18UCSC Ensembl
Cytoband3q25.1
Allele length
AssemblyAllele length
hg3882962
hg1982962
hg1882962
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv8654n54
Supporting Variantsnssv976762
Samples
Known GenesAADAC, MIR548H2, SUCNR1
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv592048
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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