A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv592489



Internal ID16379898
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:166586403..166702256hg38UCSC Ensembl
Innerchr3:166304191..166420044hg19UCSC Ensembl
Innerchr3:167786885..167902738hg18UCSC Ensembl
Cytoband3q26.1
Allele length
AssemblyAllele length
hg38115854
hg19115854
hg18115854
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1152051
SamplesNINDS_183
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv592489
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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