A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv589813



Internal ID16377222
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:15987012..16019112hg38UCSC Ensembl
Innerchr3:16028519..16060619hg19UCSC Ensembl
Innerchr3:16003523..16035623hg18UCSC Ensembl
Cytoband3p24.3
Allele length
AssemblyAllele length
hg3832101
hg1932101
hg1832101
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv959674
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv589813
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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