A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv590029



Internal ID16030752
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:30744939..30761548hg38UCSC Ensembl
Innerchr3:30786431..30803040hg19UCSC Ensembl
Innerchr3:30761435..30778044hg18UCSC Ensembl
Cytoband3p24.1
Allele length
AssemblyAllele length
hg3816610
hg1916610
hg1816610
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv960944
Samples
Known GenesGADL1
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv590029
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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