A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv589628



Internal ID16377037
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:8784055..8821239hg38UCSC Ensembl
Innerchr3:8825741..8862925hg19UCSC Ensembl
Innerchr3:8800741..8837925hg18UCSC Ensembl
Cytoband3p25.3
Allele length
AssemblyAllele length
hg3837185
hg1937185
hg1837185
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv8214n54
Supporting Variantsnssv1151850, nssv1151851
SamplesHGDP00084, HGDP00584
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv589628
Frequency
Sample Size17421
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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