A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv590969



Internal ID16378378
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:89938721..90089162hg38UCSC Ensembl
Innerchr3:89987871..90138312hg19UCSC Ensembl
Innerchr3:90070561..90221002hg18UCSC Ensembl
Cytoband3p11.1
Allele length
AssemblyAllele length
hg38150442
hg19150442
hg18150442
Variant TypeCNV gain+loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv967754, nssv967753
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv590969
Frequency
Sample Size17421
Observed Gain1
Observed Loss1
Observed Complex0
Frequencyn/a


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