A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv589881



Internal ID16377290
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:21041604..21132497hg38UCSC Ensembl
Innerchr3:21083096..21173989hg19UCSC Ensembl
Innerchr3:21058100..21148993hg18UCSC Ensembl
Cytoband3p24.3
Allele length
AssemblyAllele length
hg3890894
hg1990894
hg1890894
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv8255n54
Supporting Variantsnssv959902, nssv959901, nssv959900
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv589881
Frequency
Sample Size17421
Observed Gain3
Observed Loss0
Observed Complex0
Frequencyn/a


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