A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv592063



Internal ID16032786
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:151796802..151864407hg38UCSC Ensembl
Innerchr3:151514590..151582195hg19UCSC Ensembl
Innerchr3:152997280..153064885hg18UCSC Ensembl
Cytoband3q25.1
Allele length
AssemblyAllele length
hg3867606
hg1967606
hg1867606
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv8654n54
Supporting Variantsnssv1151809
SamplesNINDS_204
Known GenesAADAC, MIR548H2
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv592063
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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