A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv590189



Internal ID16030912
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:46755146..46799313hg38UCSC Ensembl
Innerchr3:46796636..46840803hg19UCSC Ensembl
Innerchr3:46771640..46815807hg18UCSC Ensembl
Cytoband3p21.31
Allele length
AssemblyAllele length
hg3844168
hg1944168
hg1844168
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv8304n54
Supporting Variantsnssv962551, nssv962552, nssv962550
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv590189
Frequency
Sample Size17421
Observed Gain0
Observed Loss3
Observed Complex0
Frequencyn/a


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