A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv592488



Internal ID16379897
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:166566369..166745006hg38UCSC Ensembl
Innerchr3:166284157..166462794hg19UCSC Ensembl
Innerchr3:167766851..167945488hg18UCSC Ensembl
Cytoband3q26.1
Allele length
AssemblyAllele length
hg38178638
hg19178638
hg18178638
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv8725n54
Supporting Variantsnssv981189, nssv981190
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv592488
Frequency
Sample Size17421
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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