A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv589643



Internal ID16377052
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:8804661..8813413hg38UCSC Ensembl
Innerchr3:8846347..8855099hg19UCSC Ensembl
Innerchr3:8821347..8830099hg18UCSC Ensembl
Cytoband3p25.3
Allele length
AssemblyAllele length
hg388753
hg198753
hg188753
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv8217n54
Supporting Variantsnssv958891
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv589643
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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