A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv590980



Internal ID16378389
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:90264244..90455495hg38UCSC Ensembl
Innerchr3:90313394..90504645hg19UCSC Ensembl
Innerchr3:90396084..90587335hg18UCSC Ensembl
Cytoband3p11.1
Allele length
AssemblyAllele length
hg38191252
hg19191252
hg18191252
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv8442n54
Supporting Variantsnssv967765
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv590980
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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