A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv592969



Internal ID16380378
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:195065244..195066127hg38UCSC Ensembl
Innerchr3:194785973..194786856hg19UCSC Ensembl
Innerchr3:196267262..196268145hg18UCSC Ensembl
Cytoband3q29
Allele length
AssemblyAllele length
hg38884
hg19884
hg18884
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv8823n54
Supporting Variantsnssv986701
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv592969
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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