A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv590203



Internal ID16030926
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:46769856..46808731hg38UCSC Ensembl
Innerchr3:46811346..46850221hg19UCSC Ensembl
Innerchr3:46786350..46825225hg18UCSC Ensembl
Cytoband3p21.31
Allele length
AssemblyAllele length
hg3838876
hg1938876
hg1838876
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv8307n54
Supporting Variantsnssv962600, nssv962603, nssv962601, nssv962602
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv590203
Frequency
Sample Size17421
Observed Gain0
Observed Loss4
Observed Complex0
Frequencyn/a


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