A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv590782



Internal ID16378191
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:82666192..82717637hg38UCSC Ensembl
Innerchr3:82715343..82766788hg19UCSC Ensembl
Innerchr3:82798033..82849478hg18UCSC Ensembl
Cytoband3p12.2
Allele length
AssemblyAllele length
hg3851446
hg1951446
hg1851446
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv8405n54
Supporting Variantsnssv966928
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv590782
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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