A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv590278



Internal ID16031001
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:51690131..51702728hg38UCSC Ensembl
Innerchr3:51724147..51736744hg19UCSC Ensembl
Innerchr3:51699187..51711784hg18UCSC Ensembl
Cytoband3p21.1
Allele length
AssemblyAllele length
hg3812598
hg1912598
hg1812598
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv8322n54
Supporting Variantsnssv963058
Samples
Known GenesTEX264
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv590278
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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