A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv592178



Internal ID16379587
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:162412903..162534146hg38UCSC Ensembl
Innerchr3:162130691..162251934hg19UCSC Ensembl
Innerchr3:163613385..163734628hg18UCSC Ensembl
Cytoband3q26.1
Allele length
AssemblyAllele length
hg38121244
hg19121244
hg18121244
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv8674n54
Supporting Variantsnssv977480
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv592178
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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