A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv590449



Internal ID16377858
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:63286292..63287150hg38UCSC Ensembl
Innerchr3:63271968..63272826hg19UCSC Ensembl
Innerchr3:63247008..63247866hg18UCSC Ensembl
Cytoband3p14.2
Allele length
AssemblyAllele length
hg38859
hg19859
hg18859
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv8349n54
Supporting Variantsnssv963563, nssv963562
Samples
Known GenesSYNPR
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv590449
Frequency
Sample Size17421
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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