A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv590661



Internal ID16378070
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:75379524..75547561hg38UCSC Ensembl
Innerchr3:75428675..75596712hg19UCSC Ensembl
Innerchr3:75511365..75679402hg18UCSC Ensembl
Cytoband3p12.3
Allele length
AssemblyAllele length
hg38168038
hg19168038
hg18168038
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv8382n54
Supporting Variantsnssv965668
Samples
Known GenesFAM86DP
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv590661
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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