A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv590735



Internal ID16378144
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:78873702..78928357hg38UCSC Ensembl
Innerchr3:78922852..78977507hg19UCSC Ensembl
Innerchr3:79005542..79060197hg18UCSC Ensembl
Cytoband3p12.3
Allele length
AssemblyAllele length
hg3854656
hg1954656
hg1854656
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv8393n54
Supporting Variantsnssv965827
Samples
Known GenesROBO1
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv590735
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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