A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv590662



Internal ID16378071
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:75379524..75587298hg38UCSC Ensembl
Innerchr3:75428675..75636449hg19UCSC Ensembl
Innerchr3:75511365..75719139hg18UCSC Ensembl
Cytoband3p12.3
Allele length
AssemblyAllele length
hg38207775
hg19207775
hg18207775
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv8383n54
Supporting Variantsnssv965669
Samples
Known GenesFAM86DP
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv590662
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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