A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv590114



Internal ID16377523
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:41052084..41082244hg38UCSC Ensembl
Innerchr3:41093575..41123735hg19UCSC Ensembl
Innerchr3:41068579..41098739hg18UCSC Ensembl
Cytoband3p22.1
Allele length
AssemblyAllele length
hg3830161
hg1930161
hg1830161
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv8289n54
Supporting Variantsnssv962390
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv590114
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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