A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv590183



Internal ID16030906
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:46754860..46811189hg38UCSC Ensembl
Innerchr3:46796350..46852679hg19UCSC Ensembl
Innerchr3:46771354..46827683hg18UCSC Ensembl
Cytoband3p21.31
Allele length
AssemblyAllele length
hg3856330
hg1956330
hg1856330
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv8304n54
Supporting Variantsnssv962535, nssv962537, nssv962536
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv590183
Frequency
Sample Size17421
Observed Gain0
Observed Loss3
Observed Complex0
Frequencyn/a


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