A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv589432



Internal ID16030155
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:4094550..4124049hg38UCSC Ensembl
Innerchr3:4136234..4165733hg19UCSC Ensembl
Innerchr3:4111234..4140733hg18UCSC Ensembl
Cytoband3p26.1
Allele length
AssemblyAllele length
hg3829500
hg1929500
hg1829500
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv8180n54
Supporting Variantsnssv958030
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv589432
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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