A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv590218



Internal ID16030941
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:47449330..47449906hg38UCSC Ensembl
Innerchr3:47490820..47491396hg19UCSC Ensembl
Innerchr3:47465824..47466400hg18UCSC Ensembl
Cytoband3p21.31
Allele length
AssemblyAllele length
hg38577
hg19577
hg18577
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv8309n54
Supporting Variantsnssv962955, nssv962956
Samples
Known GenesSCAP
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv590218
Frequency
Sample Size17421
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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