A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv589982



Internal ID16377391
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:26390855..26405784hg38UCSC Ensembl
Innerchr3:26432346..26447275hg19UCSC Ensembl
Innerchr3:26407350..26422279hg18UCSC Ensembl
Cytoband3p24.1
Allele length
AssemblyAllele length
hg3814930
hg1914930
hg1814930
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv8270n54
Supporting Variantsnssv960299
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv589982
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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