A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv590647



Internal ID16378056
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:75370585..75491393hg38UCSC Ensembl
Innerchr3:75419736..75540544hg19UCSC Ensembl
Innerchr3:75502426..75623234hg18UCSC Ensembl
Cytoband3p12.3
Allele length
AssemblyAllele length
hg38120809
hg19120809
hg18120809
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv8381n54
Supporting Variantsnssv965616, nssv965617
Samples
Known GenesFAM86DP
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv590647
Frequency
Sample Size17421
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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