A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv592061



Internal ID16032784
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:151796802..151836961hg38UCSC Ensembl
Innerchr3:151514590..151554749hg19UCSC Ensembl
Innerchr3:152997280..153037439hg18UCSC Ensembl
Cytoband3q25.1
Allele length
AssemblyAllele length
hg3840160
hg1940160
hg1840160
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv8653n54
Supporting Variantsnssv976836
Samples
Known GenesAADAC, MIR548H2
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv592061
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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