A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv589634



Internal ID16377043
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:8784337..8840029hg38UCSC Ensembl
Innerchr3:8826023..8881713hg19UCSC Ensembl
Innerchr3:8801023..8856713hg18UCSC Ensembl
Cytoband3p25.3
Allele length
AssemblyAllele length
hg3855693
hg1955691
hg1855691
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv8215n54
Supporting Variantsnssv1151864
Samples1798860084_A
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv589634
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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