A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv590558



Internal ID16377967
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:66864334..66889990hg38UCSC Ensembl
Innerchr3:66914758..66940414hg19UCSC Ensembl
Innerchr3:66997448..67023104hg18UCSC Ensembl
Cytoband3p14.1
Allele length
AssemblyAllele length
hg3825657
hg1925657
hg1825657
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv8364n54
Supporting Variantsnssv964223
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv590558
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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