A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv589408



Internal ID16030131
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:4019253..4218633hg38UCSC Ensembl
Innerchr3:4060937..4260317hg19UCSC Ensembl
Innerchr3:4035937..4235317hg18UCSC Ensembl
Cytoband3p26.1
Allele length
AssemblyAllele length
hg38199381
hg19199381
hg18199381
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv8174n54
Supporting Variantsnssv1152445
SamplesHGDP00133
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv589408
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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